Looking to advance your career in pharmacovigilance and drug safety operations? Syneos Health is hiring a Drug Safety Associate (Safety & PV Specialist I) for its hybrid offices in Gurugram and Hyderabad. This opportunity is ideal for professionals with 2–4 years of experience in ICSR case processing, booking & triage, spontaneous cases, clinical trial cases, and literature case handling.
If you have strong expertise in ICSR processing workflows, medical terminology, and global pharmacovigilance compliance, this role offers career progression within a globally recognized CRO environment.
About the Company
Syneos Health is a leading global biopharmaceutical solutions organization providing integrated clinical, medical affairs, and commercial services to pharmaceutical and biotechnology companies worldwide. The organization focuses on accelerating customer success through innovative clinical development and safety monitoring models.
Job Overview
- Position: Drug Safety Associate (Safety & PV Specialist I)
- Industry: Clinical Research / Contract Research
- Department: Pharmacovigilance & Drug Safety
- Employment Type: Full Time, Permanent
- Work Mode: Hybrid
- Locations: Gurugram & Hyderabad
- Salary: ₹5.5 – ₹6.5 LPA
- Experience Required: 2.5 – 4.5 Years
This Drug Safety Associate job focuses on end-to-end ICSR case processing and pharmacovigilance operations aligned with global regulatory standards.
Key Responsibilities
The selected candidate will be responsible for:
- ICSR case processing including booking and triage
- Handling Spontaneous, Clinical Trial, and Literature cases
- Ensuring compliance with global pharmacovigilance guidelines
- Performing accurate data entry and coding (MedDRA/WHO-DD familiarity preferred)
- Maintaining high-quality documentation and case narratives
- Supporting regulatory submission timelines
- Applying medical terminology knowledge in safety assessments
- Collaborating with global PV teams
This role strengthens expertise in drug safety operations, adverse event reporting, and global PV compliance frameworks.
Required Qualifications
- UG: Any Graduate
- PG: Any Postgraduate
- 2.5–4.5 years of experience in ICSR case processing
- Strong understanding of medical terminology
- Experience handling spontaneous, clinical trial, and literature cases
- Good written and verbal communication skills
- Familiarity with pharmacovigilance databases (Argus/ArisG preferred)
Why Apply for This Drug Safety Associate Role?
- Competitive salary package (₹5.5–6.5 LPA)
- Hybrid work flexibility
- Exposure to global pharmacovigilance systems
- Career growth in drug safety and PV operations
- Work with an internationally reputed CRO
Professionals aiming for long-term growth in pharmacovigilance, drug safety associate roles, ICSR processing careers, and clinical research operations should consider applying.
How to Apply
