CTI Clinical Trial and Consulting Services is a global, privately held, full-service contract research organization (CRO), delivering a complete spectrum of clinical trial and consulting services throughout the lifecycle of development, from concept to commercialization. CTI’s focused therapeutic approach provides pharmaceutical, biotechnology, and medical device firms with clinical and disease area expertise in rare diseases, regenerative medicine/gene therapy, immunology, transplantation, nephrology, hematology/oncology, neurology, infectious diseases, hepatology, cardiopulmonary, and pediatric populations. CTI also offers a fully integrated multi-specialty clinical research site that conducts phase I-IV trials. CTI has a passion for helping life-changing therapies succeed in chronically and critically ill patient populations. With clinical trial experience across 6 continents, CTI partners with research sites, patients, and sponsors to fulfill unmet medical needs. CTI is headquartered in Cincinnati, OH, with operations across North America, Europe, Latin America, and Asia-Pacific. For more information visit www.ctifacts.com

Chief Operating Officer (COO)

CTI Clinical Trial And Consulting Services

CTI Clinical Trial and Consulting Services is a global, privately held, full-service contract research organization (CRO), delivering a comp...

Perficient is the leading global digital consultancy. We imagine, create, engineer, and run digital transformation solutions that help our clients exceed customers’ expectations, outpace competition, and grow their business. With unparalleled strategy, creative, and technology capabilities, we bring big thinking and innovative ideas, along with a practical approach to help the world’s largest enterprises and biggest brands succeed.

Perficient

Perficient is the leading global digital consultancy. We imagine, create, engineer, and run digital transformation solutions that help our c...

EPAM Anywhere is a global job platform offering remote work opportunities for tech professionals.   Discover a few thousand of open remote vacancies within EPAM – one of the most advanced engineering companies in the world.   Here, you can build a career around your lifestyle, receiving competitive compensation and access to world-class learning resources while working on projects for global brands and exciting startups.    When you join Anywhere, you become a part of a community of like-minded people who committed to living life on their terms.   Join us today at anywhere.epam.com.   ____  EPAM Anywhere is a part of EPAM Systems, Inc. (NYSE: EPAM). Since 1993, EPAM has leveraged its advanced software engineering heritage to become the foremost global digital transformation services provider – leading the industry in digital and physical product development and digital platform engineering services.

EPAM Anywhere

EPAM Anywhere is a global job platform offering remote work opportunities for tech professionals.   Discover a few thousand of open remote v...

Chief Executive Officer (CEO)

American Stallion

It is a long established fact that a reader will be distracted by the readable content of a page when looking at its layout. The point of us...

Chief Technology Officer (CTO)

Global Semantic LLP

Staffing Agency

Biostaffic

Coordinates and provides the pharmaceutical care of patients for an assigned clinical unit and participates in patient care rounds with medical staff personnel. This position will establish a presence for Community Outpatient Parenteral Antimicrobial Therapy (COPAT) and related stewardship functions working under a consult agreement, as well as collaborate with infectious disease providers to manage care for HIV injectable treatments for outpatients. Responsibilities: <ul><li>Performs pharmacotherapeutic monitoring and provision of pharmaceutical care for patients in the area of service responsibility in a routine, continuous manner, taking into account the age and clinical condition of each patient.</li><li>Provides general and patient specific drug information to patients, physicians, nurses and, and other health care professionals.</li><li>Interacts routinely with physicians, nurses, and other health care professionals to provide optimal pharmaceutical care to patients.</li><li>Supports clinical pharmacist and technician educational development by participating in departmental staff development programs and provides leadership in the education of staff involved in providing pharmaceutical care to patients.</li><li>Supports clinical pharmacists in providing pharmaceutical care to patients by direct interaction, and formal educational programs. Supports and participates in pharmaceutical related research in area of specialty.</li><li>Maintains expertise in areas of practice through continual learning, journal review and other educational activities.</li><li>Educates clinical pharmacists, technicians, pharmacy students, post graduate trainees, allied health professionals, nurses and physicians in pharmacotherapy within in the specialty area. Other duties as assigned. </li></ul>Personal Protective Equipment: <ul><li>Follows standard precautions using personal protective equipment as required. </li></ul>Physical Requirements: <ul><li>Typical physical demands include ability to perform the job while standing and walking for prolonged times, approximately 75% of shift and continuously for extended periods of time. Manual dexterity sufficient to perform computer and dispensing functions of the job; ability to lift up to 30 lbs. Position often includes reaching, stretching, stooping, climbing steps and sitting. Must have normal or corrected vision. Must have ability to clearly communicate verbally by phone or in person </li></ul>Work Experience: <ul><li>Completion of a post-graduate year 2 residency (PGY2) or fellowship required or</li><li>Completion of a post-graduate year 1 residency (PGY-1) plus minimum of 2 years of experience as a clinical specialist or equivalent role which includes providing pharmaceutical care and performing pharmacotherapeutic monitoring including 50% or more of time spent in the specialty area or</li><li>Minimum of 4 years of experience as a clinical specialist or equivalent role which includes providing pharmaceutical care and performing pharmacotherapeutic monitoring including 50% or more of time spent in the specialty area. </li></ul>Complexity of Work: <ul><li>Requires critical thinking skills, decisive judgment and the ability to work with minimal supervision. Must be able to work in a stressful environment. Demonstrates a service orientation toward patients, staff, and visitors. Conveys a positive, professional image at all times. </li></ul>Certifications: <ul><li>Current State licensure as a Registered Pharmacist (RPh) or eligible for reciprocation in current State within 90 days of hire. Board Certification preferred.</li><li>For individuals required to administer immunizations, current Basic Life Support (BLS) certification through American Heart Association (AHA) and completion of a Board of Pharmacy approved course in the administration of immunizations or certification obtained within 90 days of hire are required. For individuals required to respond to adult or pediatric cardiopulmonary arrest events, current Advanced Cardiovascular Life Support (ACLS) or Pediatric Advanced Life Support (PALS) Certification through American Heart Association (AHA), or certification obtained within one (1) year of hire, is required. </li></ul>Education: <ul><li>PharmD or Bachelors of Science degree in Pharmacy from an accredited college of pharmacy and completion of a post-graduate residency or fellowship training required. If hired for a specialty area where specialty residency training is available, then specialty residency is required. </li></ul>Salaries [which may be] shown on independent job search websites reflect various market averages and do not represent information obtained directly from The Cleveland Clinic. Because we value each individual candidate, we invite and encourage each candidate to discuss salary/hourly specifics during the application and hiring process.

Coordinates and provides the pharmaceutical care of patients for an assigned clinical unit and participates in patient care rounds...

Clinical Specialist-Ambulatory Care Infectious Disease-Sign On Bonus Available

About The Role This position focuses on disease states (e.g. prostate cancer, neuroendocrine tumors, &amp; etc.) being treated by Novartis’ Radioligand Therapies. The Medical Science Liaison (MSL) role is a field based, customer-facing, non-promotional medical and scientific position. The MSL’s key objective is to create impact through advancing clinical practice within the assigned territory that leads to improved patient outcomes. The MSL must demonstrate deep therapeutic expertise, understand territory and market influences, engage scientifically with Healthcare Providers (HCPs) and medical experts, manage, and develop their territory and execute all relevant activities in alignment with the medical strategic and tactical plan – while functioning within the Novartis Code of Conduct, Ethics/Compliance policies and Working Practice documents. The MSL will Inform and shape medical strategy through application of a curious mindset to collect impactful and actionable insights, understanding the potential strategic impact of critical insights. This territory will be responsible for covering ME, NH, VT and Upstate NY. The preferable location for the successful candidate to reside would be in the Greater Albany or Rochester, NY areas. Role Responsibilities include, but are not limited to <ul><li> The MSL will leverage scientific expertise and market knowledge to establish and build professional relationships and engage with HCPs (including community physicians, pharmacists, medical experts, nurses, and other healthcare professionals) and other thought leaders in geographical area as aligned with medical strategy</li><li> The primary responsibility of the MSL is to engage with customers - customer engagements may include but are not limited to: emerging data discussions, clinical trial activities, uncovering barriers in patient journey, understanding market dynamics within their territory, exploration of areas of unmet medical need, pipeline discussions, educating on disease state and product, capturing adverse events, and capturing medical insights through all stages of product lifecycle.</li><li> Must demonstrate strategic territory vision and ensure appropriate territory identification, mapping, and planning of Medical Engagements (MEs) and Key Accounts as aligned to medical strategy and in collaboration with internal Novartis colleagues. This includes: </li></ul>a. identification of key stakeholders with influence on the patient journey and in the disease space throughout the product development lifecycle to establish strategies for education, engagement, and partnership b. identification of opportunities for partnership with academic centers, centers of excellence, and/or systems of care to drive impact within the assigned territory c. identification of opportunities to involve HCPs or MEs when a specific medical need is identified (e.g., publications, clinical trial participation, etc.) d. identification of opportunities for internal collaboration with other Novartis stakeholders to drive forward therapeutic area, clinical, or product goals as appropriate <ul><li> Provide clinical trial support for company sponsored trials facilitating relevant medical activities and working cross-functionally with Medical Affairs and Clinical Operations colleagues.</li><li> Regularly and effectively collaborates with internal colleagues (e.g., HEOR, access, marketing, commercial, sales) within the assigned therapeutic area and territory to advance clinical practice while maintaining customer centricity and a One Novartis approach in accordance with Novartis compliance standards.</li><li> Maintain in-depth knowledge of assigned therapeutic area and Novartis compounds to serve as a medical resource to customers and internal colleagues (in accordance with Working Practice Documents).</li><li> Maintain in-depth knowledge of internal policies and external regulations (e.g., field medical Working Practice Document (WPD), travel policy, expense policy, state and local laws, institutional policies) and how they affect day-to-day responsibilities.</li><li> Execute all administrative responsibilities and training (e.g., Veeva CRM, voicemail, e-mail, expense reports, compliance modules, etc.) in a timely manner, including profiling of core customers and ensuring up-to-date information in the CRM.</li><li> Champion emerging responsibilities as strategic priorities and territory needs evolve</li><li> Proactively drive personal and professional development. </li></ul>The pay range for this position at commencement of employment is expected to be between; for Manager: $158,400 - $237,600 and for AD: $183,200 - $274,800 year; however, while salary ranges are effective from 1/1/24 through 12/31/24, fluctuations in the job market may necessitate adjustments to pay ranges during this period. Further, final pay determinations will depend on various factors, including, but not limited to geographical location, experience level, knowledge, skills and abilities. The total compensation package for this position may also include other elements, including a sign-on bonus, restricted stock units, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors. [#video#https://www.youtube-nocookie.com/embed/nZeNtfM2DmA{#400,300#.#/video# EEO Statement We are Equal Opportunity Employers and take pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration and empowers our people to unleash their full potential. Accessibility and Reasonable Accommodations: Individuals in need of a reasonable accommodation due to a medical condition or disability for any part of the application process, or to perform the essential functions of a position, please let us know the nature of your request, your contact information and the job requisition number in your message: <ul><li>Novartis: e-mail us.reasonableaccommodations@novartis.com or call +1 (877)395-2339</li><li>Sandoz: e-mail reasonable.accommodations@sandoz.com or call: +1-609-422-4098 </li></ul>Role Requirements Education: Graduate degree in science or healthcare required; doctoral degree preferred (MD, PhD, DNP, PharmD, etc) Experience for Manager Level: <ul><li> 0-3 years of experience in a Field Medical position within the pharmaceutical industry or as an MSL is required OR</li><li> 3-5 years of relevant medical affairs, clinical research, or related experience in a scientific or clinical setting preferred. Previous experience in assigned or related therapeutic area is preferred. </li></ul>Experience for AD Level: <ul><li> Minimum of 3 years’ experience in a Field Medical-based position within the pharmaceutical industry or as an MSL is preferred OR</li><li> 5-7 years of relevant medical affairs, clinical research, or related experience in a scientific or clinical setting required. Previous experience in assigned or related therapeutic area is preferred. </li></ul>Experience all levels: <ul><li> Strong clinical knowledge including pharmacotherapy, treatment guidelines, clinical research processes, medical expert engagement strategies, and FDA promotional guidelines, regulations, and ethical guidelines applied to the pharmaceutical industry is required.</li><li> Candidates will perform their duties in accordance with applicable law, regulations, and Novartis policies.</li><li> Works within Ethics, Compliance and Promotional policies (Novartis &amp; Federal) and ensures those around him/her do the same</li><li> Works to ensure a diverse and inclusive environment free from all forms of discrimination and harassment</li><li> Adherence with Company policies, state and federal laws and regulations</li><li> Field-Based (Region: ME, NH, VT and Upstate NY). Candidate must reside within territory, or within a reasonable daily commuting distance of 50 miles from territory border.</li><li> The expectation of working hours and travel (domestic and/or international) will be defined by the hiring manager</li><li> Field based, customer-facing position majority of the time with approximately 60-70% travel required to achieve performance and business objectives (face to face, virtual, email, telephone, etc.). </li></ul>NOTE: Above level experience criteria are not an exhaustive list Why Novartis: Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture Field roles with a dedicated training period only: The individual hired for this role will be required to successfully complete certain initial training, including home study, in eight (8) or fewer hours per day and forty (40) or fewer hours per week. Field roles with a company car: Driving is an essential function of this role, meaning it is fundamental to the purpose of this job and cannot be eliminated. Because driving is an essential function of the role, you must have a fully valid and unrestricted driver’s license to be qualified for this role. The company provides reasonable accommodations for otherwise qualified individuals with medical restrictions, if an accommodation can be provided without eliminating the essential function of driving. Division US Business Unit MEDICAL AFFAIRS Work Location Albany, NY Company/Legal Entity Novartis Pharmaceuticals Functional Area Research &amp; Development Job Type Full Time Employment Type Regular Shift Work No Early Talent No

About The RoleThis position focuses on disease states (e.g. prostate cancer, neuroendocrine tumors, &amp; etc.) being treated by N...

Medical Science Liaison Prostate Radioligand Therapies ME NH VT NY

At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai’s human health care (hhc) mission. We’re a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of many innovative medicines, notably the discovery of the world's most widely-used treatment for Alzheimer’s disease. As we continue to expand, we are seeking highly-motivated individuals who want to work in a fast-paced environment and make a difference. If this is your profile, we want to hear from you. The Associate Director (AD), Alzheimer’s disease MSLs is responsible for the leadership, direction and management of the MSLs within their region. This includes providing overall guidance and direction to the MSLs to gain an understanding of the scientific landscape from KOLs/HCPs and communicate the information to key internal stakeholders across the AD/dementia portfolio of products. The Associate Director MSLs works closely with the Sr. Director MSLs to provide intelligence for medical brand strategies, to implement strategic and tactical plans based on those strategies and to provide overall support of medical brand strategies and clinical studies across the portfolio. In addition to the above leadership responsibilities, the AD will, be responsible for coaching and developing MSLs in their region. The MSLs of that region will directly report into the AD and the AD . This position will cover the Southeast region. Essential Functions <ul><li> Ensure operational excellence of the MSL team, including corporate aligned objective/tactics, cross-functional medical support, interaction with opinion leaders and facilitating clinical research to meet strategic development needs.</li><li> Provide leadership for the MSL function by participating on cross functional teams leading to strategic planning and working collaboratively with Commercial Operations including, Sales, Marketing and Medical &amp; Scientific Affairs.</li><li> Develop individual talent within the MSL team, including training, career evaluation, coaching, mentoring, performance management and talent review. Includes recruiting, hiring, and onboarding new MSLs.</li><li> Manage MSL activities related to presenting medical and scientific information and to external customers, including but not limited to, medical thought leaders, academic institutions and managed care.</li><li> Work with key professionals at the national, regional, and local level, supporting the education of key healthcare professionals with current, fair-balanced medical, scientific and HEOR information regarding Eisai’s products/pipeline and therapeutic areas.</li><li> Increase the awareness of Eisai data allowing the key healthcare professionals to make informed therapeutic decisions.</li><li> Work with investigators in a defined territory to facilitate the process for clinical trials.</li><li> Maintain and demonstrate thorough and up-to-date knowledge of disease state, study methodology, clinical information, and product data Ensure compliance with regulatory and other ethical guidelines relevant to the pharmaceutical industry, and to ensure compliance with Eisai policies &amp; procedures and standard operating procedures.</li><li> Travel (up to approx. 50%), locally across the US when required and including international travel. Drive company leased vehicle to meetings with health care providers and other appropriate stakeholders and partners. </li></ul>Requirements <ul><li>Advanced scientific terminal degree (PhD, PharmD, MD/DO)</li><li>8+ years industry or related experience, with at least 3 yrs experience in neurology.</li><li>Must have 3 years of experience within the pharmaceutical industry overseeing a Medical Science Liaison team or related function.</li><li>Prior drug launch experience as a MSL manager, is strongly preferred</li><li>Excellent interpersonal, communication, and leadership skills required.</li><li>A team player who is strategic and excels in a matrix environment. </li><li>Experience hiring, training, and successfully onboarding MSLs </li></ul>Other Skills And Abilities <ul><li>Demonstrated ability to work remotely and maintain morale of field based personnel that report into you, as well as good interaction with office based Medical Affairs and scientific staff.</li><li>Strong personal integrity and ethics. </li><li>Should have a proven track record of exceeding expectations with qualitative and quantitative metrics and driving MSL performance.</li><li>Successful collaboration with cross-functional colleagues, successfully leading in high profile situations</li><li>Strong broad-based scientific and pharmaceutical knowledge</li><li>Must possess a thorough understanding of the FDA, OIG, HIPPA, PhRMA, GCP and other international regulatory/ethical guidelines relevant to the pharmaceutical industry &amp; clinical trial conduct, and to ensure compliance with these external as well as internal Eisai guidelines and standard operating procedures.</li><li>Must be able to organize, prioritize, and work effectively in a constantly changing environment</li><li>Ability to interface effectively with a variety of technical platforms for the collection/development of field reports, slide content, strategy/review, and dissemination of medical information</li><li>Sound computer skills including applications for word processing, producing slide materials, working with spreadsheets, and other pharma platforms</li><li>Ability to safely and successfully operate a motor vehicle is required.</li><li>Possesses and maintains a valid driver’s license and clean driving record.</li><li>This is a field-based position. The employee is required to set up a home-based office within their defined territory. </li></ul>As a condition of employment and an essential function of this field-based position, applicants must be able to engage in person with HCPs and other third parties at their offices, institutions and other appropriate locations on a regular basis. In order to gain in-person access, applicants selected for the position may be required to complete third parties’ credentialing and/or entry requirements, which often include an attestation to and/or providing proof of having received certain vaccinations, including but not limited to the COVID-19 or flu vaccines. To the extent you are unable to meet certain requirements for qualifying medical (including pregnancy-related) or religious reasons, applicants must request a reasonable accommodation by contacting the Human Resources Department. #IND123 As a condition of employment and an essential function of this field-based position, applicants must be able to engage in person with HCPs and other third parties at their offices, institutions and other appropriate locations on a regular basis. In order to gain in-person access, applicants selected for the position may be required to complete third parties’ credentialing and/or entry requirements, which often include an attestation to and/or providing proof of having received certain vaccinations, including but not limited to the COVID-19 or flu vaccines. To the extent you are unable to meet certain requirements for qualifying medical (including pregnancy-related) or religious reasons, applicants must request a reasonable accommodation by contacting the Human Resources Department. Eisai Salary Transparency Language: The base salary range for the Associate Director, Medical Science Liaisons, US Neurology Medical Affairs (Alzheimer's Disease) / Southeast is from :176,600-231,700 Under current guidelines, this position is eligible to participate in : Eisai Inc. Annual Incentive Plan &amp; Eisai Inc. Long Term Incentive Plan. Final pay determinations will depend on various factors including but not limited to experience level, education, knowledge, and skills. Employees are eligible to participate in Company employee benefit programs. For additional information on Company employee benefits programs, visit https://us.eisai.com/careers-at-eisai/benefits. Certain other benefits may be available for this position, please discuss any questions with your recruiter. Eisai is an equal opportunity employer and as such, is committed in policy and in practice to recruit, hire, train, and promote in all job qualifications without regard to race, color, religion, gender, age, national origin, citizenship status, marital status, sexual orientation, gender identity, disability or veteran status. Similarly, considering the need for reasonable accommodations, Eisai prohibits discrimination against persons because of disability, including disabled veterans. Eisai Inc. participates in E-Verify. E-Verify is an Internet based system operated by the Department of Homeland Security in partnership with the Social Security Administration that allows participating employers to electronically verify the employment eligibility of all new hires in the United States. Please click on the following link for more information: Right To Work E-Verify Participation

At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregive...

Associate Director, Medical Science Liaisons, US Neurology Medical Affairs (Alzheimer's Disease) / Southeast

TravelNurseSource is working with Coast Medical Service to find a qualified Admin/Mgmt RN in Roswell, New Mexico, 88201! Pay Information $2,130 per week About The Position Coast Medical Service is a nationwide travel nursing &amp; allied healthcare staffing agency dedicated to providing an elite traveler experience for the experienced or first-time traveler. Coast is featured on Blue Pipes' 2023 Best Travel Agencies and named a 2022 Top Rated Healthcare Staffing Firm &amp; 2023 First Half Top Rated Healthcare Staffing Firm by Great Recruiters. Please note that pay rate may differ for locally based candidates. Please apply here or contact a recruiter directly to learn more about this position &amp; the facility, and/or explore others that may be of interest to you. We look forward to speaking with you! Job Requirements Required for Onboarding <ul><li>BLS</li><li>Core Mandatory Part I Exam</li><li>Core Mandatory Part II (Nursing) Exam</li><li>Core Mandatory Part III Exam</li><li>FL Education Attestation</li><li>RN Pharmacology Exam </li></ul>About Coast Medical Service Coast Medical Service is a Joint Commission certified healthcare staffing agency focused on per diem and travel nursing opportunities nationwide. Established in 1979, we are guided by our commitment to providing quality service to make it easier for healthcare providers to focus on patients. Our team works feverishly to foster a work environment where each individual is deeply valued, highly respected and given every opportunity for personal, professional and financial growth. At Coast Medical Service, we are fanatical about improving the quality of healthcare and connecting like-minded nurses with top-class facilities. We really listen and treat all our staff like family because, well, they are! As a result, Coast has grown 20x in the last 6 years and was included on the Inc. 5000 list of fastest growing private companies in America, as well as the Los Angeles Business Journal Top 100 fastest growing companies in LA.

TravelNurseSource is working with Coast Medical Service to find a qualified Admin/Mgmt RN in Roswell, New Mexico, 88201!Pay Inform...

Travel Registered Nurse - Admin/Mgmt - $2,130 / Week

Company Description Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies. Job Description Eurofins Environment Testing is seeking Laboratory Technicians in Altamonte Springs, Florida. Position Summary: The Laboratory Technician is responsible for various support tasks throughout the laboratory assigned on an as-needed basis. Sample preparation, glassware cleaning, and sample disposal are typical functions. The ideal candidate shall be a detail-oriented team-player and able to multi-task. Candidate should also have excellent communication and organizational skills. Key Position Functions: <ul><li> Extract/Digest environmental samples with organic solvent or Acid</li><li> Operate pipettors, balances, and/or graduated cylinders to measure samples volumes and weights</li><li> Prepare standards</li><li> Maintain scientific logbooks</li><li> Follow all Eurofins Standard Operating Procedures </li></ul>Qualifications Basic Minimum Qualifications: AA, AS, or BS in science or related field Basic Laboratory Experience Preferred But Not Required Authorization to work in the United States indefinitely without restriction or sponsorship Additional Information Position is full-time dayshift with overtime as needed. Candidates currently living within a commutable distance of Altamonte Springs, FL are encouraged to apply. Pay range: $17-19/hr Please note - Eurofins Environment Testing (USA) provides a compensation range for informational purposes, the actual base salary may vary based upon, but not limited to, relevant experience and skill set, base salary of internal peers, business sector, and geographic location. To learn more about Eurofins, please explore our website www.eurofinsus.com. We support your development! Do you feel you don’t match 100% of the requirements? Don’t hesitate to apply anyway! Eurofins companies are committed to supporting your career development. We embrace diversity! Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique. Sustainability matters to us! We are well on our way to achieving our objective of carbon neutrality by 2025, through a combination of emission reduction and compensation initiatives. We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we also count on our dedicated carbon reduction team to help us to achieve this goal! Find out more in our career page: https://careers.eurofins.com/ Company description: Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and Eurofins Scientific 2/2 March 2023 agroscience contract research services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2022, Eurofins generated total revenues of EUR 6.7 billion, and has been among the best performing stocks in Europe over the past 20 years. Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer. Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer. Eurofins Environment Testing Businesses in the US are routinely engaged in Federal Contracts. Federal Government vaccination mandates may apply to staff working in these businesses. Successful applicants may be required to confirm vaccination status or demonstrate eligibility for medical or religious exemptions prior to commencing employment. In addition, certain positions require travel for which vaccination is required in accordance with Eurofins policy.

Company DescriptionEurofins Scientific is an international life sciences company, providing a unique range of analytical testing s...

Laboratory Technician - Eurofins Environment Testing Southeast - Altamonte Springs, FL

Company Description Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies. Job Description Eurofins Environment Testing is seeking Laboratory Technicians in Altamonte Springs, Florida. Position Summary: The Laboratory Technician is responsible for various support tasks throughout the laboratory assigned on an as-needed basis. Sample preparation, glassware cleaning, and sample disposal are typical functions. The ideal candidate shall be a detail-oriented team-player and able to multi-task. Candidate should also have excellent communication and organizational skills. Key Position Functions: <ul><li>Extract/Digest environmental samples with organic solvent or Acid</li><li>Operate pipettors, balances, and/or graduated cylinders to measure samples volumes and weights</li><li>Prepare standards</li><li>Maintain scientific logbooks</li><li>Follow all Eurofins Standard Operating Procedures </li></ul>Qualifications Basic Minimum Qualifications: AA, AS, or BS in science or related field Basic Laboratory Experience Preferred But Not Required Authorization to work in the United States indefinitely without restriction or sponsorship Additional Information Position is full-time 2nd shift with overtime as needed. Candidates currently living within a commutable distance of Altamonte Springs, FL are encouraged to apply. Pay range: $17-19/hr Please note - Eurofins Environment Testing (USA) provides a compensation range for informational purposes, the actual base salary may vary based upon, but not limited to, relevant experience and skill set, base salary of internal peers, business sector, and geographic location. To learn more about Eurofins, please explore our website www.eurofinsus.com. We support your development! Do you feel you don’t match 100% of the requirements? Don’t hesitate to apply anyway! Eurofins companies are committed to supporting your career development. We embrace diversity! Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique. Sustainability matters to us! We are well on our way to achieving our objective of carbon neutrality by 2025, through a combination of emission reduction and compensation initiatives. We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we also count on our dedicated carbon reduction team to help us to achieve this goal! Find out more in our career page: https://careers.eurofins.com/ Company description: Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and Eurofins Scientific 2/2 March 2023 agroscience contract research services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2022, Eurofins generated total revenues of EUR 6.7 billion, and has been among the best performing stocks in Europe over the past 20 years. Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer. Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer. Eurofins Environment Testing Businesses in the US are routinely engaged in Federal Contracts. Federal Government vaccination mandates may apply to staff working in these businesses. Successful applicants may be required to confirm vaccination status or demonstrate eligibility for medical or religious exemptions prior to commencing employment. In addition, certain positions require travel for which vaccination is required in accordance with Eurofins policy.

Laboratory Technician (2nd Shift) - Eurofins Environment Testing Southeast - Altamonte Springs, FL

Company Description Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies. Job Description Eurofins Environment Testing is searching for a Courier in Altamonte Springs, FL. The Courier is responsible for the pick-up and delivery of water, soil and air samples to and from the laboratory using a company vehicle. Courier responsibilities include, but are not limited to, the following: <ul><li>Documenting, packaging and transporting samples in accordance with appropriate project-specific sampling and analysis plans/protocols</li><li>Responsible for quality control of all assignment and completing documents</li><li>Following and enforcing company health and safety policies. </li><li>Must be able to follow technical instructions and guidance. </li><li>Will assist with data collection and routine sampling as needed </li></ul>The ideal candidate would possess: <ul><li>Ability to follow GPS directions </li><li>Excellent communication (oral and written) and attention to detail</li><li>Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude</li><li>Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies </li></ul>Qualifications Basic Minimum Qualifications: <ul><li>High school diploma or equivalent. </li><li>A valid state issued driver’s license to drive delivery vehicles is required as an employee with driving responsibilities. </li><li>Must be able to operate a motor vehicle </li><li>Authorization to work in the United States indefinitely without restriction or sponsorship</li><li>Must be able to pass a drug test, driving history and background check </li></ul>Additional Information Full-time, Monday - Friday 8am - 5pm, with overtime as needed. Candidates currently living within a commutable distance of Altamonte Springs, FL are encouraged to apply. Pay rate: $17/hr Eurofins Environment Testing (USA) provides a compensation range for informational purposes, the actual base salary may vary based upon, but not limited to, relevant experience and skill set, base salary of internal peers, business sector, and geographic location. To learn more about Eurofins, please explore our website www.eurofinsus.com. We support your development! Do you feel you don’t match 100% of the requirements? Don’t hesitate to apply anyway! Eurofins companies are committed to supporting your career development. We embrace diversity! Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique. Sustainability matters to us! We are well on our way to achieving our objective of carbon neutrality by 2025, through a combination of emission reduction and compensation initiatives. We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we also count on our dedicated carbon reduction team to help us to achieve this goal! Find out more in our career page: https://careers.eurofins.com/ Company description: Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and Eurofins Scientific 2/2 March 2023 agroscience contract research services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2022, Eurofins generated total revenues of EUR 6.7 billion, and has been among the best performing stocks in Europe over the past 20 years. Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer. Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer. Eurofins Environment Testing Businesses in the US are routinely engaged in Federal Contracts. Federal Government vaccination mandates may apply to staff working in these businesses. Successful applicants may be required to confirm vaccination status or demonstrate eligibility for medical or religious exemptions prior to commencing employment. In addition, certain positions require travel for which vaccination is required in accordance with Eurofins policy.

Courier - Eurofins Environment Testing Southeast - Altamonte Springs, FL

Description Designs strategies spanning several studies required to complete goals and milestones in Clinical Development. Influences processes for the direction and strategy of projects. Assumes responsibility for direct reports including recruiting, managing, mentoring and developing scientific staff. Plays an influencing role as a subject matter expert in his/her field in Clinical Development for project teams, across functions and for senior management. Provides significant knowledge and has influence on go/no decisions within clinical studies, projects, and platforms. Possesses a knowledge of regulatory policies related to his/her function and fully understands their scientific basis. Evaluates studies and reviews clinical protocols and reports. The scope of position extends from his/her function, site, multidisciplinary project teams, and across multiple functions. As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to foster a healthy working environment, meaningful work, diversity and inclusion, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees. Duties &amp; Responsibilities <ul><li>Independently initiates and coordinates strategic scientific experiments with a predefined goal including developing new methodologies, protocols and/or test procedures that contribute to core group/research goals and reflect expert knowledge. May direct and oversee experimental study design and data analysis/results of and scientists.</li><li>Develops an understanding of clinical team goals and works effectively toward achieving them. The individual assumes departmental responsibility for projects within multi-disciplinary international development Core Teams for the effective development of biological projects. Interacts with International Project Leaders within the Core Team in reporting of project progress, including budgetary responsibilities to steering committees.</li><li>Prepares clear technical reports, publications and oral presentations. Independently communicates results in the form of reports and/or presentations. Presents responsibly and defends own work at meetings. May deliver updates to senior-level management in context of overall project goals. Contributes and presents project related topics within Regulatory forums (EMA, USDA, FDA).</li><li>Develops expertise in a specific project-relevant area or technology. May provide guidance and expertise to advance specific projects or evaluate and propose new technologies and concepts in support of multiple projects.</li><li>Keeps abreast of relevant literature. Develops visibility outside of functional area and effectively interacts scientifically with Key Opinion Leaders (KOLs) in relevant fields of concern. Effectively liaises internally with cross-functional stakeholders (Sales ' Marketing, Legal, Finance, Operations), to communicate and align expectations.</li><li>Individual should play an influencing role in project selection, technology knowledge and implementation, project management skills, resource planning, and the ability to directly interact with and influence regulatory agencies. </li><li>Complies with all applicable regulations. Ensures that work performed in area of responsibility is conducted in a safe and compliant manner. Maintains proper records in accordance with Standard Operating Procedures (SOPs) and policies.</li><li> Manages study budgets and follows internal processes to execute financial responsibility. </li></ul>Requirements <ul><li>DVM or PhD + 10 years of experience in a related field with a proven track record of successfully implementing or investigating technologies and adding value to the organization. </li><li>In lieu of DVM, will accept PhD (with significant experience in a veterinary-relevant field such as immunology and vaccine) + 10 years of experience in a related field with a proven track record of successfully implementing or investigating technologies and adding value to the organization.</li><li>Professional Training is a strong plus (Board certification for a DVM).</li><li>An analytical thinker. Excellent skills in understanding data and scientific decision processes, and in interpreting and reporting these data in well supported conclusions targeted at achieving project objectives.</li><li>Strong influence skills, being able to lead without formal authority (e.g. the Clinical team).</li><li> Research methodology experience.</li><li>Fosters innovation. A problem solver.</li><li>Outstanding communication and interpersonal skills. A collaborative team player. Values diversity and inclusion.</li><li>Possesses a customer service orientation, delivering results and executing in a fast and focused manner. </li><li>Exceptional planning and organizational skills with a quality orientation. Strives for business process excellence. </li><li>Accepts accountability and ownership.</li><li>Exhibits integrity and trust. </li><li>Willingness to travel</li><li>Clinical veterinary practice experience is preferred, with Board Certification being a strong plus.</li><li>Board Certification and/or advanced degree (MS or PhD) in addition to DVM is a strong plus.</li><li>A minimum of seven years of broad experience in a related field with a proven track record of successfully implementing or investigating technologies and adding value to the organization or an equivalent combination of education and experience. </li><li>Demonstrates industry-leading knowledge of field. </li><li>Ability to communicate effectively both orally and in writing in an inter-disciplinary and international environment.</li><li>Leadership experience: 5-7 years leading projects</li><li>Demonstrated knowledge of the Pharmaceutical/Biological life cycle process.</li><li>Experienced in project/program management. </li><li>Research methodology experience. </li></ul>Eligibility Requirements: <ul><li>Must be legally authorized to work in the United States without restriction.</li><li>Must be willing to take a drug test and post-offer physical (if required).</li><li>Must be 18 years of age or older. </li></ul>

DescriptionDesigns strategies spanning several studies required to complete goals and milestones in Clinical Development. Influenc...

Clinical Livestock Project Lead

Sarepta Therapeutics is seeking a highly motivated individual with expertise in bioanalytical method development using molecular and histological assays. The Research Associate II, Translational Biology will support the day-to-day testing of biological samples from clinical and pre-clinical trials in accordance with the requirements of approved protocols and regulatory guidance. The Research Associate will have strong expertise in molecular and histological assays and utilize this experience to perform early and late stage assay development, qualification and validation, assay execution. The Research Associate will support data recording, summarization, and reporting. The Research Associate will contribute to assay development, validation and clinical and pre-clinical sample testing to support ongoing clinical trials. Additional responsibilities include contributing to laboratory compliance and inspection readiness activities and drafting methods, SOPs, protocols and technical reports. Primary Responsibilities Include <ul><li>Conduct sample analysis in accordance with GLP/GCLP standards using a variety of assay formats including ddPCR, western blot, SimpleWestern, immunohistochemistry/immunofluorescence, and ELISA.</li><li>Responsible for managing project deliverables and timelines. Will coordinate activities and timelines in close collaboration with the laboratory team(s), Clinical Operations, Data Management, Biostatistics, and CROs.</li><li>Support the development, validation and implementation of bioanalytical methods for new and/or improved clinical biomarker assays.</li><li>Support the preparation of written test protocols and study reports and support data transfer and analysis in collaboration with intramural and extramural teams.</li><li>Responsible for sample logistics and data management across multiple clinical and non-clinical trials.</li><li>Support digital image acquisition, morphometric image analysis and interpretation.</li><li>Support the onboarding and qualification of new equipment and software.</li><li>Assist in training new employees on technical procedures as assigned in standard methods, practices, procedures, and equipment operations.</li><li>Completing general lab tasks, preventive maintenance and quality control, maintain a clean working area and adhere to proper safety techniques and procedures while ensuring compliance with GCP/GCLP guidelines. Assist in maintaining laboratory compliance and inspection readiness. </li></ul>Desired Education And Skills <ul><li>Bachelor’s degree in a chemical, physical or biological science with 3+ years of experience in healthcare, biotech/pharmaceutical industry or equivalent.</li><li>Ability to execute sample handling and analysis with strict adherence to laboratory methods, and SOPs using Good Documentation Practices (GDP)</li><li>Working knowledge of biomedical research methodologies including PCR, Western Blot and ELISA.</li><li>Knowledge of histology and immunohistochemical techniques</li><li>Proven scientific leadership when working with collaborative, multi-functional teams and troubleshooting complex laboratory processes.</li><li>Desire to work in a dynamic, fast-paced, high functioning and collaborative team environment and to make a difference in the lives of people through innovative medicines</li><li>Ability to work extended hours as needed, including but not limited to weekend and holiday coverage, occasionally on short notice</li><li>Experience and/or willingness to be trained in necropsy procedures </li></ul>This position requires work on site at one of Sarepta’s facilities in the United States. The targeted salary range for this position is $68,000 - $85,000 per year. Sarepta is making a good faith effort to be transparent and accurate around our hiring ranges. The salary offer is commensurate with Sarepta’s compensation philosophy and considers factors including, but not limited to, education, training, experience, external market conditions, criticality of role, and internal equity. Candidates must be authorized to work in the U.S. Sarepta Therapeutics offers a competitive compensation and benefit package. Sarepta Therapeutics is an Equal Opportunity/Affirmative Action employer and participates in e-Verify.

Sarepta Therapeutics is seeking a highly motivated individual with expertise in bioanalytical method development using molecular a...

Research Associate II

Cambridge Isotope Laboratories, Inc. is seeking a Packaging Technician I based onsite in our Andover, MA location. As the leading company in a niche scientific market, CIL works with cutting-edge researchers in clinical diagnostics, proteomics, environmental testing, protein discovery, drug development, metabolomics and industrial research. CIL has had consistent growth and profitability for over 40 years. CIL's growing customer base spans academia, pharmaceutical and chemical industry, enabling collaborations with Nobel laureates and industry-leading scientists and chemists. CIL partners with leading instrument manufacturers and pioneering research groups with expertise in product development.Packaging Technicians are responsible for weighing, dispensing, bottling, packaging and labeling GMP, ISO and non-GMP product from bulk storage in preparation for shipping or warehousing. Responsibilities<ul><li>Weigh and measure product to be dispensed according to PSO. </li></ul><ul><li>Manually, or through operation of automated packaging equipment, dispense and package chemical products (e.g. dry, solvents, gas) into appropriate containers (e.g. NMR tubes, ampoules, cylinders, bottles, boxes) per Packaging Shop Order (PSO) specification. </li><li>Inspect, box and seal containers. Where necessary using flame torches. </li><li>Label packaged product.</li><li>Transport packaged goods to shipping or finished goods warehouse.</li> </ul><ul><li>Carry out duties with due consideration of safety and good housekeeping per CIL's Safety Manual.</li><li>Perform other related duties and responsibilities as may be required. </li> </ul>Requirements <ul><li>High School Diploma or General Education Degree (GED) with a minimum of 2 years of closely related experience working with chemical products or, equivalent education or specialized training.</li><li>Associate's or Bachelor's degree in the sciences preferred. </li><li>Must be able to weigh and measure product using metric system, operate flame torch and demonstrate manual dexterity.</li><li>Complete documentation with high level of accuracy.</li><li>Regularly requires sitting, standing, bending and lifting or moving of up to 50 - 100 pounds.</li><li>Requires use of handheld flame torch.</li><li>In accordance with CIL safety requirements, may perform packaging tasks in a hooded, controlled environment with personalized safety equipment.</li><li>Employees work with hazardous and non-hazardous chemicals.</li> </ul>Benefits CIL offers a competitive salary and a comprehensive benefit program including generous paid time off, health insurance with no in-network deductibles, multiple Long Term Incentives and 6% matching 401K plan.CIL is an EEO/Affirmative Action employer.Learn more about us on our website: www.isotope.com About us:Cambridge Isotope Laboratories, Inc. (CIL) is the world's leading producer of stable isotopes and stable isotope-labeled compounds. With nearly 600 employees and laboratories in four countries, CIL specializes in the process of labeling biochemical and organic compounds with highly enriched, stable (nonradioactive) isotopes of carbon, hydrogen, nitrogen and oxygen. Our chemists substitute common atoms (e.g., 1H, 12C, 14N, 16O) with rare, highly valued isotopes (e.g., 2H or D, 13C, 15N, 18O) so that the final product can be readily measured or traced using mass spectrometry (MS) or nuclear magnetic resonance (NMR). CIL's products are utilized in laboratories, medical, government and academic research centers and health care facilities worldwide.We are proud that CIL products have contributed to medical advancements in cancer research, new-drug development, environmental analysis, and medical diagnostic research. In the past decade, as the fields of proteomics and metabolomics have developed as leading techniques for determining biomarkers for disease presence, progression and the monitoring of therapeutic response, CIL has worked closely with industry leaders and researchers to provide the stable isotope-labeled tools needed for improved quantitation and qualification of complex biological systems.After decades of research, stable isotopes have found their place in an ever expanding commercial scale applications in pharmaceuticals, semiconductors, flat panel displays as well as other high technology fields specifically with deuterium oxide (D2O) and deuterium gases. Pharmaceutical companies have begun to investigate deuteration of molecules that may provide advantages over their existing nondeuterated counterparts. In addition, increasing research into the potential medical advantages of new deuterated drugs is also occurring. In high technology, deuterated organic molecules and deuterium gas are commonly used in the manufacturing of microelectronics and OLEDs, which contribute to the increased lifetime of the devices.Learn more about us on our website: www.isotope.com

Cambridge Isotope Laboratories, Inc. is seeking a Packaging Technician I based onsite in our Andover, MA location. As the leading ...

Packaging Technician I

Panoramic Health Come Join our team!! Clinical Research Coordinator I will perform delegated duties such as protocol required visit procedures, administering questionnaires and subject material, administering, and dispensing medication, adhering to regulatory guidelines, and participating in subject recruitment efforts, under the oversight of the study Principal Investigator. The Clinical Research Coordinator needs to engage with the Principal Investigators, pharmaceutical companies (Sponsors) and contract research organizations (monitors) as well as the research subjects. Responsibilities Include <ul><li> Read and understand assigned research protocols. Prescreen patients. Train site staff on study purpose, record attendance. Evaluate resources needed and on-hand to appropriately deploy the study. </li><li> Drive enrollment to meet contractual targets: Using the EMR, screen for eligible patients for discussion and qualification by the Principal Investigator. Obtain and document informed consent per ICH/GCP and site SOPs. Timely, clean data entry according to ALCOA principle (“Attributable, Legible, Contemporaneous, Original and Accurate”). </li><li> Prepare for monitoring visits: All Source Documents organized and readily available. All outstanding items from prior monitoring visit are resolved. No open queries from prior visit. Temperature and accountability logs readily available. </li><li> Ongoing Study oversight and management: Plan subject visits according to protocol specific visit schedule. No protocol deviations due to out of window procedures. Communication with location administration to make sure space and other resources are available as needed. Reporting of Adverse and Serious Adverse Events to IRB and Sponsor in accordance with reporting guidelines. Dispensing/collecting study medication and providing accurate Investigational Product accountability. Collecting and processing subject laboratory specimens according to protocol. Completing case report forms (CRFs) and other patient tracking information (either electronic or manual) accurately and on a timely basis as assigned. Maintaining a thorough understanding of all data collection instruments and collecting data accurately and according to protocol. </li><li> Perform other duties and responsibilities as required, assigned, or requested. </li></ul>Qualifications <ul><li> Bachelors’ degree required; Nursing or Health Science preferred. </li><li> Bilingual preferred (Spanish). </li><li> Minimum 2 years’ experience as a clinical research coordinator. </li><li> Therapeutic area experience in CKD, nephrology, or vascular access a plus. </li><li> Knowledge of and adherence to Good Clinical Practice (GCP), IATA and FDA regulations. </li><li> Must be able to do basic clinical procedures such as: blood work, vitals, height, weight, etc. </li><li> Must be able to do an ECG. </li><li> Travel to Investigator meetings or other study locations is expected with this position. Travel might be outside the local area and overnight. </li></ul>The Company is committed to the principles of equal employment. We are committed to complying with all federal, state, and local laws providing equal employment opportunities, and all other employment laws and regulations. It is our intent to maintain a work environment which is free of harassment, discrimination, or retaliation because of age, race, color, national origin, ancestry, religion, sex, pregnancy (including childbirth, lactation and related medical conditions), physical or mental disability, genetic information (including testing and characteristics), veteran status, uniformed servicemember status, or any other status protected by federal, state, or local laws. The company is dedicated to the fulfillment of this policy in regard to all aspects of employment, including but not limited to recruiting, hiring, placement, transfer, training, promotion, rates of pay, and other compensation, termination, and all other terms, conditions, and privileges of employment For information about our Privacy Policy, please visit here Apply Now

Panoramic HealthCome Join our team!!Clinical Research Coordinator I will perform delegated duties such as protocol required visit ...

Clinical Research Coordinator - Arlington, VA

Company Description Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies. Job Description Eurofins Environment Testing is seeking a Sample Receiving Disposal Technician in Atlanta, GA. Responsibilities include <ul><li>Proper disposal of samples. </li><li>Maintaining cleanliness and organization in the waste disposal room and loading dock area including waste removal throughout the day. </li><li>Properly utilizing personal protective equipment at all times while disposing of samples. </li><li>Load and unload pallets/ boxes/ materials. </li><li>Assist with sample transfer between departments within the laboratory. </li><li>Assist Sample Custodian with sample location as well as returning samples to cooler in proper storage locations (temperature = 4˚C) for 3-4 hours per day. </li><li>Organize samples located in waste disposal room. </li><li>Help clean and organize coolers. </li><li>Remove samples from coolers to table, &amp; sort them accordingly</li><li>Learn &amp; become knowledgeable of bottle types, sample test codes and preservatives</li><li>Must adhere to analytical and quality control protocols described in SOP’s, the QA Manual, and project specific requirements. </li></ul>Will assist with other assigned projects as needed. Qualifications Basic Minimum Qualifications: Education: <ul><li>High school diploma or GED. </li><li>AA degree in a life or physical science (biology, chemistry, environmental studies, etc.) preferred. </li></ul>Authorization to work in the United States indefinitely without restriction or sponsorship Ability to lift up to 30 lbs. Detail oriented, flexible, dependable, with a willingness to learn new things Must be a team player and have good communication and organizational skills Additional Information Position is full-time, Monday – Friday 8:30 am - 5:30 pm with overtime as needed. Candidates currently living within a commutable distance of Atlanta, GA are encouraged to apply. Pay rate: $18/hr Eurofins Environment Testing (USA) provides a compensation range for informational purposes, the actual base salary may vary based upon, but not limited to, relevant experience and skill set, base salary of internal peers, business sector, and geographic location. To learn more about Eurofins, please explore our website www.eurofinsus.com. We support your development! Do you feel you don’t match 100% of the requirements? Don’t hesitate to apply anyway! Eurofins companies are committed to supporting your career development. We embrace diversity! Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique. Sustainability matters to us! We are well on our way to achieving our objective of carbon neutrality by 2025, through a combination of emission reduction and compensation initiatives. We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we also count on our dedicated carbon reduction team to help us to achieve this goal! Find out more in our career page: https://careers.eurofins.com/ Company description: Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and Eurofins Scientific 2/2 March 2023 agroscience contract research services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2022, Eurofins generated total revenues of EUR 6.7 billion, and has been among the best performing stocks in Europe over the past 20 years. Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer. Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer. Eurofins Environment Testing Businesses in the US are routinely engaged in Federal Contracts. Federal Government vaccination mandates may apply to staff working in these businesses. Successful applicants may be required to confirm vaccination status or demonstrate eligibility for medical or religious exemptions prior to commencing employment. In addition, certain positions require travel for which vaccination is required in accordance with Eurofins policy.

Sample Disposal Technician - Eurofins Environment Testing Southeast - Atlanta, GA

TravelNurseSource is working with Coast Medical Service to find a qualified Home Health RN in Monroe, Georgia, 30655! Pay Information $2,362 per week About The Position Coast Medical Service is a nationwide travel nursing &amp; allied healthcare staffing agency dedicated to providing an elite traveler experience for the experienced or first-time traveler. Coast is featured on Blue Pipes' 2023 Best Travel Agencies and named a 2022 Top Rated Healthcare Staffing Firm &amp; 2023 First Half Top Rated Healthcare Staffing Firm by Great Recruiters. Please note that pay rate may differ for locally based candidates. Please apply here or contact a recruiter directly to learn more about this position &amp; the facility, and/or explore others that may be of interest to you. We look forward to speaking with you! Job Requirements Required for Onboarding <ul><li>BLS</li><li>Core Mandatory Part I Exam</li><li>Core Mandatory Part II (Nursing) Exam</li><li>Core Mandatory Part III Exam</li><li>FL Education Attestation</li><li>Home Health Care-Medication Exam</li><li>Home Health RN Exam</li><li>Home Health RN Skills Checklist</li><li>RN Pharmacology Exam </li></ul>About Coast Medical Service Coast Medical Service is a Joint Commission certified healthcare staffing agency focused on per diem and travel nursing opportunities nationwide. Established in 1979, we are guided by our commitment to providing quality service to make it easier for healthcare providers to focus on patients. Our team works feverishly to foster a work environment where each individual is deeply valued, highly respected and given every opportunity for personal, professional and financial growth. At Coast Medical Service, we are fanatical about improving the quality of healthcare and connecting like-minded nurses with top-class facilities. We really listen and treat all our staff like family because, well, they are! As a result, Coast has grown 20x in the last 6 years and was included on the Inc. 5000 list of fastest growing private companies in America, as well as the Los Angeles Business Journal Top 100 fastest growing companies in LA.

TravelNurseSource is working with Coast Medical Service to find a qualified Home Health RN in Monroe, Georgia, 30655!Pay Informati...

Travel Nurse RN - Home Health - $2,362 / Week

Company Description Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies. Job Description Eurofins Environment Testing is seeking a Sample Receiving Disposal Technician in Atlanta, GA. Responsibilities include <ul><li>Proper disposal of samples.</li><li>Maintaining cleanliness and organization in the waste disposal room and loading dock area including waste removal throughout the day.</li><li>Properly utilizing personal protective equipment at all times while disposing of samples.</li><li>Load and unload pallets/ boxes/ materials.</li><li>Assist with sample transfer between departments within the laboratory.</li><li>Assist Sample Custodian with sample location as well as returning samples to cooler in proper storage locations (temperature = 4˚C) for 3-4 hours per day.</li><li>Organize samples located in waste disposal room.</li><li>Help clean and organize coolers.</li><li>Remove samples from coolers to table, &amp; sort them accordingly</li><li>Learn &amp; become knowledgeable of bottle types, sample test codes and preservatives</li><li>Must adhere to analytical and quality control protocols described in SOP’s, the QA Manual, and project specific requirements. </li></ul>Will assist with other assigned projects as needed. Qualifications Basic Minimum Qualifications: Education <ul><li>High school diploma or GED.</li><li>AA degree in a life or physical science (biology, chemistry, environmental studies, etc.) preferred. </li></ul>Authorization to work in the United States indefinitely without restriction or sponsorship Ability to lift up to 30 lbs. Detail oriented, flexible, dependable, with a willingness to learn new things Must be a team player and have good communication and organizational skills Additional Information Position is full-time, Monday – Friday 8:30 am - 5:30 pm with overtime as needed. Candidates currently living within a commutable distance of Atlanta, GA are encouraged to apply. Pay rate: $18/hr Eurofins Environment Testing (USA) provides a compensation range for informational purposes, the actual base salary may vary based upon, but not limited to, relevant experience and skill set, base salary of internal peers, business sector, and geographic location. To learn more about Eurofins, please explore our website www.eurofinsus.com. We support your development! Do you feel you don’t match 100% of the requirements? Don’t hesitate to apply anyway! Eurofins companies are committed to supporting your career development. We embrace diversity! Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique. Sustainability matters to us! We are well on our way to achieving our objective of carbon neutrality by 2025, through a combination of emission reduction and compensation initiatives. We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we also count on our dedicated carbon reduction team to help us to achieve this goal! Find out more in our career page: https://careers.eurofins.com/ Company description: Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and Eurofins Scientific 2/2 March 2023 agroscience contract research services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2022, Eurofins generated total revenues of EUR 6.7 billion, and has been among the best performing stocks in Europe over the past 20 years. Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer. Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer. Eurofins Environment Testing Businesses in the US are routinely engaged in Federal Contracts. Federal Government vaccination mandates may apply to staff working in these businesses. Successful applicants may be required to confirm vaccination status or demonstrate eligibility for medical or religious exemptions prior to commencing employment. In addition, certain positions require travel for which vaccination is required in accordance with Eurofins policy.

At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai’s human health care (hhc) mission. We’re a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of many innovative medicines, notably the discovery of the world's most widely-used treatment for Alzheimer’s disease. As we continue to expand, we are seeking highly-motivated individuals who want to work in a fast-paced environment and make a difference. If this is your profile, we want to hear from you. Job Summary The Manager, Field Training will be responsible for effectively pulling through training strategies, resources and initiatives via coaching and field rides, new hire training and supplemental training initiatives including regional training sessions/programs for field sales representatives in their assigned geography within the U.S (U.S. to be divided between the respective positions). This full-time role will be responsible for mentoring and training newly hired representatives, providing skill-building for tenured representatives and supporting the Commercial Training and Development Team throughout the year. The Manager, Field Training will partner with Sales Training, Field Sales and Marketing teams to compile and deliver training programs and materials that meet the defined and specific needs of the Neurology sales force. The Manager, Field Training will travel throughout their assigned geography in the U.S. to deliver the aforementioned. The position is a Commercial Training &amp; Development role that will report into the Director, Alzheimer’s Disease Training, and will have strong collaboration and relationships with the home office Sales Training Team ad Field Sales Leadership Team. Essential Functions <ul><li>Pull-through training strategy, initiatives and resources via coaching and field rides </li><li>Provide New Hire Training support during homestudy, initial training and post-training </li><li>Conduct supplemental training initiatives including but not limited to virtual web trainings, teleconferences, National/Regional/District meetings. </li><li>Align field coaching to the Selling Model to further enhance field execution. </li><li>Provide written feedback via FCRs to provide appropriate coaching</li><li>Ensure field pull-through is consistently aligned to brand/training initiatives throughout respective regions</li><li>Funnel continuous feedback into Commercial Training team to inform future curriculum and content</li><li>Conduct special projects, assignments and other functions the job may require to perform </li></ul>Requirements <ul><li>Bachelor’s degree required</li><li>Minimum of 5 years pharmaceutical sales experience</li><li>Strong desire to coach, mentor and develop new hires and peers</li><li>Demonstrated strong leadership skills, initiative and business planning skills</li><li>Understanding of Neurology therapeutic area and current trends preferred</li><li>Strong understanding of pharmaceutical industry procedures and regulations</li><li>Strong written and verbal communication skills</li><li>Superior sales, product and disease state expertise</li><li>Ability to work independently and multi-task</li><li>Demonstrated commitment to and understanding of broader organization objectives and positive mindset</li><li>Travel up to 75% of the time </li></ul>#IND123 As a condition of employment and an essential function of this field-based position, applicants must be able to engage in person with HCPs and other third parties at their offices, institutions and other appropriate locations on a regular basis. In order to gain in-person access, applicants selected for the position may be required to complete third parties’ credentialing and/or entry requirements, which often include an attestation to and/or providing proof of having received certain vaccinations, including but not limited to the COVID-19 or flu vaccines. To the extent you are unable to meet certain requirements for qualifying medical (including pregnancy-related) or religious reasons, applicants must request a reasonable accommodation by contacting the Human Resources Department. Eisai Salary Transparency Language: The base salary range for the Field Training Manager, Alzheimer's Disease (Southeast) (Field Based) is from :111,800-146,700 Under current guidelines, this position is eligible to participate in : Eisai Inc. Annual Incentive Plan. Final pay determinations will depend on various factors including but not limited to experience level, education, knowledge, and skills. Employees are eligible to participate in Company employee benefit programs. For additional information on Company employee benefits programs, visit https://us.eisai.com/careers-at-eisai/benefits. Certain other benefits may be available for this position, please discuss any questions with your recruiter. Eisai is an equal opportunity employer and as such, is committed in policy and in practice to recruit, hire, train, and promote in all job qualifications without regard to race, color, religion, gender, age, national origin, citizenship status, marital status, sexual orientation, gender identity, disability or veteran status. Similarly, considering the need for reasonable accommodations, Eisai prohibits discrimination against persons because of disability, including disabled veterans. Eisai Inc. participates in E-Verify. E-Verify is an Internet based system operated by the Department of Homeland Security in partnership with the Social Security Administration that allows participating employers to electronically verify the employment eligibility of all new hires in the United States. Please click on the following link for more information: Right To Work E-Verify Participation

Field Training Manager, Alzheimer's Disease (Southeast) (Field Based)

Peachtree BioResearch Solutions is a specialized full-service CRO that "thinks like a sponsor". Formed almost 15 years ago by a leadership team experienced in buying CRO service while at a global pharma, our operational teams are highly experienced and bring valuable insight for our small sponsor clients - no matter their budget. We do this by investing in people who thrive in an environment where their experience and insight can be leveraged beyond their main functional area. This is a great environment for people who want to do more. Summary: Peachtree BioResearch Solutions is looking to add a Principal Clinical Data Manager to our team. This person will report to the Director, Clinical Data Management. This a fully remote position open to candidates in the United States. The selected candidate will be responsible for activities associated with the acquisition, documentation, review, cleaning, and processing of clinical data, collected for investigational and marketed drugs, in clinical trials. What You'll Do: The Principal Clinical Data Manager (CDM) will have responsibilities that include, but are not limited to: <ul><li>Performing/managing the responsibilities associated with the acquisition, documentation, review, cleaning, and processing of clinical data collected for marketed and investigational drugs, in clinical trials. As a member of the clinical study team, relay information regarding data management status, knowledge regarding area of discipline, and timelines affecting Data Management deliverables.</li><li>Ensuring the accuracy and consistency of Case Report Forms and databases designed according to Sponsor specifications, and Clinical Protocol.</li><li>Creating the Data Management Plan, Edit Check Specifications, and Data Management Report while ensuring consistency with the Clinical Trial Protocol and follow internal or sponsor procedures, international or national regulations and Good Clinical Practices.</li><li>Projecting, planning, developing, implementing, and delivering quality results in a timely manner. This will require the use of data, measurements and a systematic approach and is accomplished specifically by:</li><ul><li>Interpreting the Clinical Protocol to ensure the accurate and efficient design of the CRF.</li><li>Analyzing metrics surrounding the activities associated with the acquisition, documentation, review, cleaning, and processing of clinical data.</li><li>Interpreting study timelines and prioritizing workload appropriately.</li></ul><li>Coordinating and managing the activities of a CDM trial team, typically comprised of Clinical Programmers, Clinical Data Associates and Coding Specialists. This includes reviewing and approving all documents issued by the Clinical Data Management trial team.</li><li>Participating in Clinical Data Management initiatives, to contribute to the continuous improvement of the processes and technologies utilized within the department.</li><li>Ensuring Data Management tasks are performed according to the work orders, which describes the specific CDM activities and time for completion, contracted with the Sponsor Company and central laboratory, while ensuring adherence to federal regulations, Good Clinical Practice and Good Clinical Data Management Practices. </li></ul>What We Think You Need to be Successful in this Role: <ul><li>Minimum of 8 years clinical data management experience, preferably in pharmaceutical research and development or related field.</li><li>Bachelor's degree in a life sciences field, preferred.</li><li>Experience and ability to work independently, as well as manage several diverse projects simultaneously, under tight time constraints.</li><li>Ability to engage and demonstrate cooperative behavior to lead team efforts.</li><li>Experience in responding rapidly to changing priorities and in managing aggressive deadlines.</li><li>Excellent written and verbal communication skills. Extensive experience in communicating with all levels of personnel, in domestic and international environments.</li><li>Demonstrated experience in leading and participating in collaborative work teams.</li><li>Strong leadership abilities and interpersonal skills.</li><li>Accurately and efficiently work toward quality results, creation of new processes and procedures, and decision-making based on precedent, company policies, federal regulations, Good Clinical Practice and Good Clinical Data Management Practices.</li><li>Independent decision making and implementation.</li><li>Excellent communication, organization, problem solving and project management skills.</li><li>Working knowledge of medical terminology, federal regulations, Good Clinical Practice, CDISC standards and Good Clinical Data Management Practices. </li></ul>In addition to working on some great teams, full-time employees will get: <ul><li>Medical, Dental, Vision coverage (Company contributes significantly to premiums)</li><li>20 days PTO + 13 Paid Holidays</li><li>100% employer matching 401(k)</li><li>Short &amp; Long-term disability benefits</li></ul>

Peachtree BioResearch Solutions is a specialized full-service CRO that "thinks like a sponsor". Formed almost 15 years ago by a le...

Principal Clinical Data Manager

Peachtree BioResearch Solutions is a specialized full-service CRO that "thinks like a sponsor". Formed almost 15 years ago by a leadership team experienced in buying CRO service while at a global pharma, our operational teams are highly experienced and bring valuable insight for our small sponsor clients - no matter their budget. We do this by investing in people who thrive in an environment where their experience and insight can be leveraged beyond their main functional area. This is a great environment for people who want to do more. Summary: Peachtree BioResearch Solutions is looking to add a Senior Clinical Data Associate to our team. This person will report to the Manager, Clinical Data Management. This a fully remote position open to candidates in the United States. The selected candidate will be responsible for leading the efforts to perform data cleaning activities, including data quality assurance checks on clinical data collected for investigational drugs in clinical trials, to ensure data is of high quality and ready for statistical analysis. What You'll Do: The Senior Clinical Data Associate (CDA) will have responsibilities that include, but are not limited to: <ul><li>Acting as a CDA leader in reviewing and interpreting automated data discrepancy output, as well as performing manual listing reviews and generating data queries to be sent to the investigational site, following standard conventions and procedures.</li><li>Managing the data cleaning process for the study, including interpreting clinical site responses to queries, and determining whether the responses are sufficient.</li><li>Proactively updating the clinical database with the resolution provided and determining the resolution status of the queries, for studies using paper-based processes.</li><li>Leading the efforts in regular status updates to the Clinical Data Manager regarding data cleaning efforts to facilitate an expeditious database lock.</li><li>Performing quality control measures to ensure the final clinical database is prepared for analysis and reporting as specified in the Data Management Plan.</li><li>Participating in system and study validation processes, including the creation and execution of validation test documentation.</li><li>Creating trial specific documentation as needed, such as CRF Completion Guidelines.</li><li>Providing support for study team and investigational site staff regarding Electronic Data Capture systems.</li><li>Initiating and participating in Clinical Data Management initiatives, to contribute to the continuous improvement of the standard processes and technologies utilized within the department.</li><li>Assisting with data processor activities during times of peak workload.</li><li>Providing data management trial support for the study Clinical Data Manager. </li></ul>What We Think You Need to be Successful in this Role <ul><li>Minimum 3 - 5 years clinical data review/cleaning experience, preferably in pharmaceutical research and development or related field.</li><li>Preferred experience with relational databases, preferably Electronic Data Capture (EDC) systems.</li><li>Oracle Clinical, Rave, or Inform systems preferred. </li><li>Knowledge of computer system validation, in particular FDA 21 CFR part 11, desired.</li><li>Must demonstrate the ability to interpret, evaluate and trouble-shoot issues pertaining to the data associate activities, to determine the appropriate actions necessary for ensuring that the tasks associated with cleaning are completed both accurately and efficiently.</li><li>Working knowledge of federal regulations, Good Clinical Practice, and Good Clinical Data Management Practices.</li><li>Excellent communication skills, both verbal and written, of English.</li><li>Accurately and efficiently work towards quality results.</li><li>Ability to work independently, as well as handle multiple diverse projects simultaneously, under tight time constraints.</li><li>Independent decision making and implementation.</li><li>Exceptional knowledge of MS Office products.</li><li>Excellent communication, time-management, and organizational skills. </li></ul>In addition to working on some great teams, full-time employees will get: <ul><li>Medical, Dental, Vision coverage (Company contributes significantly to premiums)</li><li>20 days PTO + 13 Paid Holidays</li><li>100% employer matching 401(k)</li><li>Short &amp; Long-term disability benefits</li></ul>

Senior Clinical Data Associate

About UsWe are a leading regenerative medicine company in the advanced and acute wound care space and are always looking for exceptional talent. Join a company where you will have an opportunity to grow professionally and personally and give strength to others by Empowering Healing. Our advanced wound care products are specially developed for the successful treatment of chronic and acute wounds. Our comprehensive portfolio of skin substitutes and other regenerative medicine products empower our patients with life-changing solutions. Our strength is giving others strength. What You Will Achieve:The Medical Science Liaison (MSL) at Organogenesis is a clinical and scientific expert representing the Medical Science team. The MSL is responsible for communicating clinical and scientific product information to the healthcare community in an ethical and unbiased manner through one-on-one interactions, small group discussions and lecture presentations. The MSL will manage the educational and scientific needs of Key Opinion Leaders (KOL's) by establishing long-term strategic relationships. Leveraging their relationships and knowledge of wound healing, the MSL will provide strategic input and operational support for clinical development programs.The candidate must have good interpersonal skills and the ability to work in a cross functional matrixed organization. This position will focus activities in the Mid Atlantic area. This will include the following states: VA, NC, SC, TN, KY, and GA. Ideal candidate will live in the territory and close to a major airport. How You Will Achieve It:<ul><li>In cooperation with the Medical Information Center, respond to requests for clinical and scientific information related to Organogenesis’s products.</li><li>Develop and prepare educational slide decks which are presented to various external customers.</li><li>Remain current on the developments and trends in medical sciences. Attend assigned local, regional, and national medical symposiums. Assist with publication planning and execution initiatives. Run gap analyses to inform publication strategy.</li><li>Provide broad clinical and scientific support for commercial team activities. This would include input on product positioning as well as medical based training for the commercial team members.</li><li>When requested, provide a review of data on potential new business development opportunities.</li><li>Follow up on post-marketing adverse events by obtaining relevant clinical information to enable the Medical Director to make an accurate assessment. Follow up may also involve re-education regarding effective &amp; safe product usage.</li><li>Identify potential investigators for clinical development programs and interact with them on an ongoing basis.</li></ul> What You Need to Achieve It:Must have excellent communication skills, both written and oral. Clinical experience in the wound healing field is preferred. Must have effective project management, leadership, interpersonal, analytical, and problem-solving skills. Must be able to work independently and in groups in a collegial manner. Must be able to travel up to 80% (4 days a week).<ul><li>Minimum of 2 years’ experience as a health care provider, MSL, or in the wound care field. A master’s degree or higher is required.</li><li>Experience serving as a medical professional in a medical device, biotechnology or pharmaceutical company is desirable.</li><li>Demonstrated ability to communicate effectively and confidently with experts and/or opinion leaders in the field of wound care.</li><li>Good understanding of the wound healing marketplace and current/investigational treatment options in this therapeutic area.</li><li>Clinical and/or research experience in the therapeutic area of wound healing is desirable.</li><li>Ability to provide education on complex clinical and scientific topics in a clear and concise manner.</li><li>Strong working knowledge of the Microsoft Office Suite (Word, PowerPoint, Excel).</li></ul> What can we offer you?<ul><li>401k -- generous employer match with immediate vesting and financial planning resources</li><li>Comprehensive Medical, Dental and Vision coverage options effective on day one of employment</li><li>Flexible Spending Account (medical expenses or dependent care expenses) or Health Savings Account</li><li>Company paid insurances including Short Term, Long Term and Life insurances as well as voluntary options</li><li>Paid maternity leave and parental leave for all new parents</li><li>Adoption benefits</li><li>Education Assistance Policy - $5,000 per year for all employees</li><li>Wellness Program including free trainings on mental health, mindfulness, stress reduction, on-site flu shots and more</li><li>Employee Assistance Program</li><li>Generous paid time off including vacation, floating holidays, sick days, and company holidays</li><li>Free parking including an electric charging station (Canton and La Jolla)</li><li>Discounts at BJs Wholesale, Dell, Sullivan Tire, and Sprint</li></ul> We are an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to age, sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, genetic information or any other characteristic protected by law.

About UsWe are a leading regenerative medicine company in the advanced and acute wound care space and are always looking for excep...

Medical Science Liaison

Tempus – Southeast - Regional Sales Manager Passionate about making a difference in the world of cancer genomics? With the advent of genomic sequencing, we can finally decode and process our genetic makeup. We now have more data than ever before but providers don't have the infrastructure or expertise to make sense of this data. We're on a mission to connect an entire ecosystem to redefine how genomic data is used in clinical settings. Position Overview: Tempus’s Southeast Regional Sales Manager (RSM) will be responsible for leading a Regional Sales Team (Tennessee, Georgia and Northeast Florida) and to exceeding sales goals across Tempus’s product portfolio. This encompasses the creation and implementation of regional and territory business plans as well as the selection, hiring, training, development, and management of Clinical Account Executives within a defined geographic region. The RSM will be responsible for managing business results, sales activities, and cross functional initiatives in a specific regional geography. Responsible for making the day to day decisions required to manage a business function including deploying resources, allocating costs, and directing business activities. Securing and analyzing relevant information, knowledge of region, market intelligence, environmental factors and political landscape, to identify key issues and committing to action after developing alternative solutions that take into consideration strategic objectives, resource constraints and organizational values. This is a front-line sales management/leadership position covering several states requiring frequent travel to work with Account Executives in their assigned territories. Responsibilities <ul><li>Achievement of regional sales objectives; revenue and expenses.</li><li>Development and execution of a regional and territory business plans.</li><li>Direct execution of sales strategies and tactics, and implementation of sales and marketing plans.</li><li>Develop and maintain key customer relationships with target audiences; assist in developing business solutions that are mutually beneficial; apply broader business scenarios and customer-focused models to achieve breakthrough results.</li><li>Plan and conduct regional sales meetings designed to inform and convey existing and new product knowledge and applications and enhance and develop sales and business skills.</li><li>Evaluate performance of Clinical Account Executives</li><li>Maintain high level of product and market knowledge.</li><li>Identify contracting opportunities with academic medical centers, large cancer centers, health systems, and other strategically important key accounts.</li><li>Management oversight of Tempus’s CRM solution for the defined geographic region.</li><li>Work collaboratively with cross-functional partners to access resources and maximize outcomes. </li></ul>Required Skills <ul><li>Deep domain knowledge of the Diagnostic Services industry. Molecular Diagnostic experience strongly preferred.</li><li>Experience selling Oncology based tests and services into the Pathology and/or Oncology clinical communities preferred.</li><li>Experience within complex selling environments required.</li><li>Demonstrated success in recruiting, hiring, developing and retaining talent.</li><li>Ability to prioritize and align organizational goals and objectives; enable innovation.</li><li>Ability to develop and utilize cross-functional relationships to facilitate the accomplishment of work goals and objectives.</li><li>Ability to provide an integrated MolDx/SaaS solution using Tempus’s sequencing technology to prospects and customers.</li><li>Ability to engage in a consultative selling process that overcomes objections and indifferences while connecting client needs with Tempus’s capabilities.</li><li>Comfortable selling at the executive level (CEO, COO, CFO)</li><li>Keen understanding of the payor and reimbursement environment in the oncology and diagnostic space</li><li>Ability to work independently, communicate proactively, manage multiple projects and prioritize daily tasks while managing critical deadlines</li><li>Problem solving, decision making and technical learning.</li><li>Advanced written and oral communication skills.</li><li>Strong administrative skills. Sophistication to manage business in complex environments.</li><li>Knowledge and application of strategic planning, and development sales strategy and tactical implementation.</li><li>Experience and understanding of managing the financial dynamics of a commercial organization.</li><li>Expertise in health care with emphasis on molecular diagnostics, genomics, biotechnology, pharmaceuticals, and oncology.</li><li>Superior listening and problem solving skills</li><li>Ability to handle sensitive information and maintain a very high level of confidentiality</li><li>Demonstrate consistent closing abilities throughout the sales cycle</li><li>Possess a very positive attitude and an understanding of the dynamics involved with organizational growth and change</li><li>Impeccable oral and verbal communication and presentation skills</li><li>Must be very proficient with all Microsoft Office products – particularly Excel and PowerPoint</li><li>Effective and regular utilization of Salesforce.com</li><li>Ability to develop and utilize cross-functional relationships to facilitate the accomplishment of work goals and objectives.</li><li>Advanced presentation skills and business acumen a necessity</li><li>Demonstrate Tempus’ Values by acting with integrity, respect and trust and representing our company culture at all time to external and internal constituents</li><li>Frequent travel ( ~50%) throughout the territory as needed </li></ul>Required Education And Experience <ul><li>A minimum of 5-years’ experience in a relevant industry/commercial environment (pharmaceutical, diagnostics, research products) as a sales manager, leading a team of 8+ reps</li><li>Bachelor’s degree required, MBA preferred.</li><li>A track record of success in a management role </li></ul>Note To Employment Agencies Tempus values our relationships with our recruitment partners and will only accept resumes from those partners whom have been contracted by a member of our Human Resources team to collaborate with us. Tempus is not responsible for any fees related to resumes that are unsolicited or are received by any employee of Tempus who is not a member of the Senior Leadership team. We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

Tempus ? Southeast - Regional Sales ManagerPassionate about making a difference in the world of cancer genomics?With the advent of...

Regional Sales Manager - Southeast

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