Datakaar
br{display:none;}.css-58vpdc ul > li{margin-left:0;}.css-58vpdc li{padding:0;}]]>
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]