GE HealthCare Technologies is seeking a Medical Director for Global Pharmacovigilance to lead drug safety and risk management activities. The ideal candidate will have significant experience in pharmacovigilance, particularly in medical review and safety signal detection
Job Summary
The role provides medical leadership across proactive safety surveillance and lifecycle risk management activities within Global Pharmacovigilance.
The incumbent serves as a Subject Matter Expert for global regulations including ICH, EU, and US guidelines while preparing key regulatory documents.
GE HealthCare offers a culture fostering care, collaboration, and support with total rewards designed to unlock ambition.
Matching Summary
Match Score: 85
GE HealthCare Technologies is seeking a Medical Director for Global Pharmacovigilance to lead drug safety and risk management activities. The ideal candidate will have significant experience in pharmacovigilance, particularly in medical review and safety signal detection.
Skills & Requirements
Must-have
5 years pharmaceutical PV experience
Medical review of Individual Case Safety Reports
Knowledge of FDA EU ICH regulations
MedDRA coding and WHO DD dictionary skills
Safety signal detection and evaluation
Nice-to-have
Global experience preferred
Strong oral and written communication
Project management skills
Cross-functional collaboration abilities
Problem analysis and resolution
Key Requirements
Minimum 5 years pharmaceutical/biotechnology PV experience
Proven ability to assess Individual Case Safety Reports
Expertise in MedDRA term assignment and WHO DD coding