The role is responsible for managing various medical affairs projects assigned by the medical director, including financial oversight and cross-functional communication
Job Summary
The role is responsible for managing various medical affairs projects assigned by the medical director, including financial oversight and cross-functional communication.
Candidates must consolidate and draft Risk Management Plan (RMP) documentation required by health authorities and write clear case narratives summarizing adverse events.
The position involves coordinating new or ongoing Real-World Evidence (RWE) projects while ensuring compliance with standard processes, policies, and budget milestones.
Matching Summary
The role is responsible for managing various medical affairs projects assigned by the medical director, including financial oversight and cross-functional communication.
Salary
Not specified; Not specified; Not specified
Skills & Requirements
Must-have
Previous pharmaceutical operational experience
Project management experience in medical affairs
RMP documentation consolidation and drafting
Adverse event narrative writing skills
Cross-functional communication capabilities
Nice-to-have
Demonstrated agility in fast-paced environments
Experience with RWE project coordination
Strong English verbal and written communications
Audit experience within pharmaceutical sector
Vendor communication and management skills
Key Requirements
Advanced degree in medical sciences or related discipline
2+ years' experience in the pharmaceutical industry
Basic experience in clinical research and study management
Pharmacist or related degree preferred
Extensive knowledge in study operational processes