Experience: 8 - 12 years.
Job type: Permanent.
Roles and Responsibility:
-
Familiar with Pharmacovigilance Risk Management Plan (RMP) processes
-
Familiar with Pharmacovigilance Periodic Safety Reports (PSR) processes
-
Experience in transfer of business requirements into technical specifications
-
Experience with Top-30 Pharma companies
- Cross-functional experience safety / pharmacovigilance and regulatory affairs
-
Good to have experience with Veeva.RIM
-
Good to have experience with Feith Orbit platform
-
Strong organization and verbal/written communication skills
Please share your updated resumes on
[email protected]