Advanced scientific degree (MD, PhD, PharmD, NP or similar) with relevant scientific background required
Experience supporting publication activities, literature review, or evidence generation projects.
Familiarity with advisory board processes, content management systems, and medical / regulatory compliance frameworks.
Proficiency in medical literature databases (e.g., PubMed, Embase) and Microsoft Office Suite.
Working knowledge of pharmaceutical compliance requirements, including PhRMA Code and FDA regulations.
Experience working within an international company with a complex organizational environment
Ability to travel up to 30%
