Syneos Health is inviting applications for the position of Safety & Pharmacovigilance Coordinator in Gurugram and Hyderabad (Office-Based). Candidates with 1+ year of Pharmacovigilance experience in Clinical Trial (CT) or Literature case processing are encouraged to apply.
This Pharmacovigilance job opportunity is ideal for B.Pharm, M.Pharm, PharmD, or BDS graduates seeking career growth in drug safety case processing, ICSR data entry, and safety database management within a global CRO environment.
With operations in over 110 countries and involvement in 94% of novel FDA-approved drugs in the last five years, Syneos Health provides strong exposure to global regulatory standards including ICH-GCP, GVP modules, and global drug safety regulations.
🔎 Job Overview
- Position: Safety & Pharmacovigilance Coordinator
- Location: Gurugram / Hyderabad
- Job Type: Full-Time (Office-Based)
- Experience Required: Minimum 1 Year in Pharmacovigilance (Case Processing/Data Entry Mandatory)
- Preferred Experience: Clinical Trial (CT) & Literature Case Processing
🧾 Key Responsibilities – Pharmacovigilance Coordinator
The Safety & Pharmacovigilance Coordinator will:
- Monitor and route incoming safety information to project teams
- Perform accurate ICSR data entry and case processing in safety databases
- Track and record all safety documentation per sponsor guidelines
- Redact patient-identifiable data as per ICH-GCP and GVP requirements
- Support literature and clinical trial (CT) case processing
- Assist in translation coordination for safety source documents
- Support query follow-up and safety submission processes
- Maintain case files (electronic and paper)
- Conduct daily workflow reconciliation activities
- Follow SOPs, WIs, global PV regulations, and study plans
This role requires precision in pharmacovigilance data entry, safety database systems, MedDRA coding knowledge, and regulatory compliance documentation.
🎓 Eligibility & Qualifications
Educational Qualification
- B.Pharm / M.Pharm / PharmD / BDS
Experience
- Minimum 1 year of Pharmacovigilance case processing or full data entry role (mandatory)
- Experience in Clinical Trial (CT) cases and Literature cases preferred
- Knowledge of safety databases and medical terminology preferred
Technical Skills
- MS Office (Word, Excel, PowerPoint, Outlook)
- Familiarity with document management systems
- Understanding of ICH Guidelines, GVP Modules, and global drug safety regulations
Soft Skills
- Strong documentation accuracy
- Ability to manage multiple tasks
- Team collaboration
- Willingness to work rotational shifts
🌟 Why Join Syneos Health?
- Exposure to global drug safety operations
- Career progression in Pharmacovigilance and Clinical Research
- Supportive line management & therapeutic training
- Competitive total rewards program
- Opportunity to work on studies involving FDA and EMA approved products
Syneos Health promotes diversity, inclusion, and professional development in a fast-paced global CRO environment.
💰 Salary (Estimated)
Based on industry standards for 1–3 years Pharmacovigilance experience:
₹3.2 LPA – ₹5.5 LPA (Approximate CTC Range)
(Final salary depends on experience and interview performance.)
📩 How to Apply
