Medical Key Opinion Leader - Remote

Job Title: Medical Key Opinion Leader
Location: Remote UK/EU
Contract length: 6 months
Contract type: Freelance
Please note you must be able to work in the EU or UK without restriction or sponsorship to be eligible for this role. If you are interested in finding out more about this role or others, please contact Manpreet Bhullar at mbhullar@i-pharmconsulting.com or call UK: +44 (0)20 7551 0802 / EU: +31 20 809 0665.
I-Pharm Consulting are partnering with one of the largest companies in the Baltic states with 50 years of experience in the production of medicines and chemical pharmaceutical products. The range of product portfolio developed by the company, which is continuously developed and expanded, includes 60 finished dosage forms, 25 active pharmaceutical substances and more than 20 intermediates, including medicinal products for the nervous system, cardiovascular health, as well as antiviral, antibacterial and anti-allergic drugs. They are looking for a Key Opinion Leader to join them and bring their expert opinion on new product ideas.
Description
The appointed KOL will play a crucial role in evaluating therapeutic areas such as antidiabetics, cardiology, neurology, and oncology. The primary objective is to propose innovative generics by considering modifications to dosage forms, dosage adjustments, and combinations of various molecules. The client already possesses a list of candidates and concepts that they wish to evaluate in collaboration with the KOL, as initial steps to determine the viability of ongoing collaboration. Ideally, the KOL should possess both clinical and academic experience. The consultant, being a seasoned medical professional, will provide expert opinions on new product ideas that aim to:

• Enhance patient compliance
• Increase treatment adherence
• Reduce medication costs
• Explore additional indications for already available drugs
  

The Key Tasks To Be Undertaken Include

• Conducting a comprehensive medical assessment of proposed new products, incorporating a literature review.
• Assisting in the preparation of scientific advice packages and responding to agency questions.
• Welcoming proposals from the KOL's perspective.
• Developing a clinical trial pathway.
• Providing advice on the regulatory pathway for the drug approval process.
• Assisting in building awareness for the product after submission and approval.
• Addressing clinical questions from the agency.
• Assisting in designing the product profile and labelling.
• Additional tasks may be discussed based on the unique requirements of individual products.