Looking for an exciting Pharmacovigilance Specialist job in India? Syneos Health is inviting applications for Safety & Pharmacovigilance Specialist I/II (ICSR) positions in Gurugram and Hyderabad. Professionals with 2.6 to 6.5 years of experience in ICSR case processing, Argus, ArisG, Drug Safety, and Pharmacovigilance are encouraged to apply.
This is an excellent opportunity for experienced pharmacovigilance professionals who want to work with one of the world’s leading clinical research organizations while contributing to global drug safety and regulatory compliance.
Job Details
| Particular | Details |
|---|---|
| Position | Safety & Pharmacovigilance Specialist I / II |
| Company | Syneos Health |
| Experience | 2.6–6.5 Years |
| Job Type | Full-Time |
| Work Mode | Work From Office |
| Shift | Regular Shift |
| Locations | Gurugram, Hyderabad |
| Vacancies | 15 |
| Salary | ₹4.8 – ₹6.5 LPA (Approx.) |
As a Pharmacovigilance Specialist, you will be responsible for:
- Perform end-to-end ICSR case processing.
- Process spontaneous, clinical trial, and literature cases.
- Conduct medical data entry with high accuracy.
- Perform MedDRA coding and WHO Drug coding.
- Prepare medical narratives.
- Execute case triage activities.
- Ensure submission readiness of safety cases.
- Perform quality control (QC) of processed cases.
- Maintain compliance with global pharmacovigilance regulations.
- Follow SOPs, GVP guidelines, and regulatory timelines.
- Collaborate with cross-functional pharmacovigilance teams.
- Deliver high-quality work within agreed timelines.
Applicants should possess any of the following:
- 2.6–6.5 years in Pharmacovigilance
- Strong ICSR Case Processing experience
- Hands-on experience with Argus Safety Database
- Experience in ArisG Safety System
- Knowledge of Drug Safety regulations
- Understanding of global Pharmacovigilance compliance
- Literature case processing experience preferred
- Quality review (QC) experience is an advantage
- Pharmacovigilance
- Drug Safety
- ICSR Processing
- Argus Safety
- ArisG
- MedDRA Coding
- WHO Drug Dictionary
- Clinical Trial Safety
- Literature Cases
- Narrative Writing
- Patient Safety
- PMS
- Spontaneous Case Processing
- Regulatory Reporting
- Workflow Management
Working at Syneos Health offers professionals an opportunity to:
- Work with global pharmaceutical clients.
- Gain exposure to international pharmacovigilance standards.
- Enhance expertise in ICSR processing.
- Build experience in quality review activities.
- Advance your career in Drug Safety.
- Work in a structured and compliant environment.
- Learn from experienced pharmacovigilance professionals.
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