Posted:1 week ago| Platform:
On-site
Part Time
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 connect@datakaar.com
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Salary: Not disclosed
Salary: Not disclosed