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Medical Affairs Recruitment

EPM Scientific exists to enable exceptional careers around the world; we connect exceptional talent, with exceptional opportunities. EPM Scientific is focused on providing the highest quality candidate search service available on the market. We specialize in locating and attracting niche talent, exclusively focused on Life Sciences, offering Contract, Permanent, Project Based and Multi-Hire Recruitment Solutions.

Our Medical Affairs team mirrors the demands of our clients and candidates, we identify, qualify and present the highest caliber candidates, as well as identifying the best permanent and contract opportunities for leading Adaptive Technology professionals across the globe. 

In recent years; the focus of policy makers, buyers and patients has shifted from the price of a product to the value of a product. This has caused a substantial change in the expectations of those within Medical Affairs, who are now required to have a much
broader skill set. Medical Affairs teams are expected to work closer than ever with internal teams: Research and Development, Market Access and Regulatory Affairs – in order to combine clinical and medical results with patient outcomes; whilst adding value to a variety of external stakeholders.

As a result, not only are candidate expected to have an exceptional educational background, but also to understand the commercial element of successfully delivering a product to market. These individuals combine the intelligence and knowledge of
the development process with the commercial ability to meet the varied demands of external stakeholders. As a result, they become one of the key players behind FDA and EMA approvals and without the right people; the vast investments made in the clinical process will not be utilized.

Latest jobs

Manager of Regulatory Affairs
  • Job type: Permanent
  • Location: Cambridge, Massachusetts
  • Salary: US$120000 - US$150000 per year
  • Description My client is a best-in-class viral vector contract development and manufacturing organization (CDMO) for companies developing gene-modified cell therapies and in vivo gene therapies
Director, Pharmacovigilance Operations
  • Job type: Permanent
  • Location: Basking Ridge, New Jersey
  • Salary: US$180000 - US$220000 per year
  • Description Director, Pharmacovigilance Operations Northern, New Jersey A medium-sized biopharmaceutical company focused becoming the industry leader in Oncology is seeking a dynamic Director
Project Manager, Regulatory Affairs
  • Job type: Permanent
  • Location: San Diego, California
  • Salary: US$70000 - US$100000 per year
  • Description Project Manager, Regulatory Affairs Looking for a Project Manager, Regulatory Affairs for one of my largest Biopharmaceutical clients in San Diego! The Project Manager is responsible for
Director of Business and Contract Management
  • Job type: Permanent
  • Location: Malmö
  • Salary: Competitive
  • Description Director of Business & Contract Management, Malmo, Sweden
Project Manager, Regulatory Affairs
  • Job type: Permanent
  • Location: San Diego, California
  • Salary: Competitive
  • Description Title: Project Manager, Regulatory Affairs Company summary: A leading, global, bio-pharmaceutical organization is looking for an experienced professional to join their Regulatory Operations team in
Associate Director of Regulatory Operations
  • Job type: Permanent
  • Location: San Diego, California
  • Salary: Competitive
  • Description Title: Associate Director, Regulatory Operations Company summary: A leading, global, bio-pharmaceutical organization is looking for an experienced professional to join their Regulatory Operations team