Kickstart Your PV Career as a Safety & PV Specialist I at Syneos Health | Pharmacovigilance jobs
If you’re searching for Pharmacovigilance Jobs or exploring growth opportunities in Syneos Health Careers, the role of Safety & PV Specialist I is an excellent fit. Based in Hyderabad, this position is ideal for professionals looking for PV Jobs in Hyderabad with hands-on expertise in ICSR case processing, safety reporting, and global PV systems. Join Syneos Health and be part of a global team committed to transforming patient safety and advancing biopharmaceutical innovation.
Job Details:
- Job Position: Safety & PV Specialist I
- Location: Hyderabad, India – Hybrid
About the Company
Syneos Health® is a global biopharmaceutical solutions leader supporting breakthrough research and development. As part of the expanding landscape of Syneos Health Careers, the organization empowers talent across 110 countries. With 29,000 employees, Syneos Health delivers integrated clinical and commercial expertise and fosters a Total Self culture rooted in diversity, inclusion, and authenticity, perfectly aligning with those searching for pharmacovigilance career paths.
Job Description | Pharmacovigilance Jobs
The Safety & PV Specialist I role is central to advancing patient safety and regulatory compliance. As part of the expanding ecosystem of Pharmacovigilance Jobs within Syneos Health Careers, this position involves processing Individual Case Safety Reports (ICSRs), ensuring data accuracy, managing safety databases, and supporting global PV operations from the Hyderabad center—one of the most active regions for PV Jobs in Hyderabad.
Key Responsibilities in Pharmacovigilance Jobs
- Perform ICSR case processing including booking, triage, and data entry.
- Enter information into PVG quality and tracking systems.
- Evaluate ICSR completeness, regulatory reportability, and narrative compilation.
- Code events, medical history, tests, and concomitant medications.
- Generate expedited regulatory reports as required.
- Conduct literature screening, MedDRA coding, and maintain drug dictionary.
- Manage xEVMPD product records and manual recoding tasks.
- Identify & manage duplicate ICSRs. In these roles, pharmacovigilance is a core focus.
- Perform safety tracking and quality reviews of ICSRs.
- Ensure documentation for TMF and PSMF is properly maintained.
- Adhere to SOPs, WIs, GCP, ICH, GVP, and project safety plans.
- Participate in audits and collaborate with cross-functional teams.
Qualifications:
- Education: B. Pharm, M. Pharm, BDS, BMS, MBBS (No BSc/MSc accepted).
- Experience: 2.5–4 years in pharmacovigilance/safety roles.
- Tools: Argus Database, Aris-G.
- Strong knowledge of PV regulations and ICSR processes.
