
Medical Affairs, Medical Information & PV Introduction

Medical Affairs teams are commonly referred to as the scientific bridge between the industry and stakeholders. The activities conducted by the Medical Affairs teams are post-approval focused, with primary obligations to provide scientific and clinical support for commercial products. Essentially, Medical Affairs professionals will communicate the complex data gathered from the clinical trials to healthcare professionals and stakeholders.
This complex data is communicated through various methods/materials to educate healthcare professionals about the product. For example, educational information, reports and discussions with industry practitioners. Medical Affairs teams are responsible for reviewing these materials to ensure that they comply with the Association of British Pharmaceutical Industry (ABPI) code of practice. In addition to these key responsibilities, a Medical Affairs team manages the relationship with key opinion leaders (KOLs).
We recruit for the following roles within Medical Affairs, Medical information & PV:
- Head of Medical Affairs / Medical Director / Associate Director
- Medical Lead / Therapy Area Lead
- Medical Advisor / Senior Medical Advisor
- Medical Science Liaison
- Medical Affairs Manager
- Medical Information Officer / Specialist / Manager
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A career in Medical Affairs, Medical Information & PV
What should I do to progress in my career in this sector?
f you are seeking to progress your career within Medical Affairs, you must assemble a broad skillset and gather relevant industry experience. In addition to this, you will need to complete several key tasks to accelerate your career progression. As a minimum, you will hold a PhD.
Often Pharmacy and medical degrees are the requirement but not at all times. Researching the sector will enable you to gain a better understanding of industry policies and best practices to be successful within your job role. Medical Affairs teams are responsible for reviewing communication materials developed by their company. Once these materials have been reviewed and approved, a senior-level professional within the team will then ‘’sign them off’’. To have the authority to do this, you will need to have gained the final signatory certification. It is only possible to be a final signatory if you are a pharmacist of GMC registered physician
Continuing professional development (CPD) allows professionals to identify gaps in their capabilities and knowledge. By addressing these through regular training, you will become more efficient within your job role.
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