Syneos Health is hiring Safety & Pharmacovigilance (PV) Coordinators for its Hyderabad office. This is an excellent opportunity for B.Pharm and M.Pharm professionals with at least 1 year of experience in Pharmacovigilance (PMS & Spontaneous Case Processing) to build a rewarding career with one of the world’s leading clinical research organizations.
The role focuses on ICSR processing, case triage, MedDRA coding, literature screening, safety database management, expedited reporting, xEVMPD submissions, TMF documentation, and regulatory compliance. Candidates with Argus or LSMV experience and strong knowledge of ICH-GCP, GVP, and post-marketing safety are encouraged to apply.
If you’re looking for Syneos Health Pharmacovigilance Jobs 2026, Drug Safety Jobs in Hyderabad, or ICSR Processing Jobs, this opportunity offers excellent career growth within global clinical development.
Job Overview
| Particular | Details |
|---|---|
| Company | Syneos Health |
| Position | Safety & PV Coordinator |
| Job Type | Full-Time |
| Work Mode | Office-Based |
| Location | Hyderabad, India |
| Eligibility | B.Pharm / M.Pharm |
| Experience | Minimum 1 Year |
| Preferred Experience | PMS & Spontaneous Case Processing |
| Safety Database | LSMV (Argus acceptable) |
| Application Deadline | 05 August 2026 |
Key Responsibilities
The selected Safety & PV Coordinator will:
- Process Individual Case Safety Reports (ICSRs)
- Perform case intake, triage and safety tracking
- Review ICSRs for completeness and regulatory reportability
- Enter safety data into pharmacovigilance databases
- Perform MedDRA coding for adverse events and indications
- Code concomitant medications and medical history
- Prepare complete narrative summaries
- Conduct literature screening and safety review
- Generate and submit expedited safety reports
- Perform duplicate ICSR identification and reconciliation
- Support xEVMPD product record validation and submissions
- Assist with SPOR and IDMP related activities
- Conduct quality review of safety cases
- Maintain Trial Master File (TMF) documentation
- Ensure compliance with SOPs, ICH-GCP, GVP and global regulatory requirements
- Participate in audits and quality inspections
- Collaborate with internal and external project teams
Eligibility Criteria
Candidates must have:
- B.Pharm or M.Pharm degree
- Minimum 1 year of Pharmacovigilance experience
- Experience handling PMS and Spontaneous Cases
- Knowledge of ICSR processing lifecycle
- Experience with Argus or LSMV Safety Database
- Good understanding of:
- ICH-GCP
- Good Pharmacovigilance Practices (GVP)
- Clinical Trials (Phase II-IV)
- Post-Marketing Safety
- Knowledge of MedDRA coding
- Strong communication and documentation skills
- Microsoft Office proficiency
Preferred Skills
- Pharmacovigilance Operations
- Drug Safety Case Processing
- Medical Terminology
- Expedited Reporting
- Narrative Writing
- MedDRA Coding
- Literature Screening
- Signal Support
- TMF Documentation
- xEVMPD Validation
- SPOR / IDMP
- Duplicate Case Management
- Quality Review
- Regulatory Compliance
Why Join Syneos Health?
Syneos Health is among the world’s largest clinical research organizations, supporting pharmaceutical, biotechnology, and medical device companies throughout drug development.
Benefits include:
- Global pharmacovigilance exposure
- Career progression opportunities
- Continuous technical training
- International projects
- Collaborative work environment
- Exposure to global regulatory requirements
- Employee recognition programs
- Strong learning and development culture
Who Should Apply?
This opportunity is ideal for:
- B.Pharm graduates
- M.Pharm graduates
- Pharmacovigilance Associates
- Drug Safety Executives
- ICSR Processing Professionals
- Case Processing Specialists
- Safety Database Executives
- Professionals seeking Hyderabad Pharmacovigilance Jobs
How to Apply
