Offer summary
Qualifications:
RN, MS, MPH, PharmD or equivalent degree, Minimum 15 years of drug development experience, Experience in phase 1 to phase 3 programs, Strong understanding of PV processes, Experience with ArisGlobal LSMV and Veeva Vault preferred.
Key responsabilities:
- Oversee drug safety operations and activities
- Manage safety database systems and processes
- Collaborate with external vendors for safety case processing
- Ensure compliance with regulatory reporting for drug safety
- Serve as a subject matter expert in pharmacovigilance