Protiviti India Member Firm is currently hiring Life Science graduates for Drug Safety / Pharmacovigilance roles in Chennai. This opportunity is ideal for B.Pharm, M.Pharm, and Pharm.D graduates looking to begin their career in pharmacovigilance, drug safety case processing, and global safety database management.
The role focuses on adverse event case processing, safety data management, regulatory compliance, and pharmacovigilance operations aligned with global regulatory standards.
With hybrid work mode and structured shifts, this position provides pharmacy graduates a strong entry point into the global drug safety and pharmacovigilance industry.
Job Overview
| Category | Details |
|---|---|
| Position | Drug Safety Associate / Pharmacovigilance Associate |
| Company | Protiviti India Member Firm |
| Location | Chennai, India |
| Work Mode | Hybrid |
| Shift Timings | Morning (6 AM โ 3 PM), Evening (3 PM โ 12 AM) |
| Qualification | B.Pharm, M.Pharm, Pharm.D |
| Experience | Freshers / Entry Level |
| Industry | Pharmacovigilance / Drug Safety |
Key Responsibilities
Selected candidates will work on pharmacovigilance case processing and drug safety monitoring activities.
Main responsibilities include:
- Identification and creation of safety cases in the Global Safety Database
- Managing incoming safety information from intake workflow, client mailbox, and electronic gateways
- Triage and prioritization of safety cases according to regulatory timelines
- Performing case processing and data entry for adverse events
- Submission and follow-up of serious and non-serious adverse event reports
- Maintaining compliance with client SOPs and global pharmacovigilance regulations
- Tracking follow-up information and case updates
- Ensuring accurate drug safety documentation and reporting
These activities support global pharmacovigilance operations and regulatory drug safety compliance.
Eligibility Criteria
Candidates interested in this Protiviti pharmacovigilance job should meet the following criteria:
Educational Qualification
- B.Pharm
- M.Pharm
- Pharm.D
Preferred Skills
- Basic knowledge of Pharmacovigilance and Drug Safety
- Understanding of Adverse Event (AE) and Serious Adverse Event (SAE) reporting
- Knowledge of global safety databases
- Familiarity with ICH guidelines and regulatory requirements
- Strong data entry and documentation skills
- Good communication and analytical abilities
Why This Role is Valuable for Pharma Graduates
This Drug Safety Associate role at Protiviti offers a strong foundation in pharmacovigilance operations.
Career advantages include:
- Exposure to global drug safety databases
- Hands-on experience with case processing and adverse event reporting
- Work in a global pharmacovigilance environment
- Opportunity to develop regulatory compliance expertise
- Entry pathway into Drug Safety, Pharmacovigilance, and Clinical Research careers
Many professionals who start in pharmacovigilance case processing roles later move into positions such as:
- Drug Safety Scientist
- Safety Data Analyst
- Signal Detection Specialist
- Pharmacovigilance Manager
Work Mode and Shifts
Protiviti offers hybrid working options for this role.
Shift timings include:
- Morning Shift: 6:00 AM โ 3:00 PM
- Evening Shift: 3:00 PM โ 12:00 AM
These shifts align with global pharmacovigilance operations and international regulatory timelines.
Salary (Estimated)
Based on entry-level pharmacovigilance roles in India, the expected salary range may be:
โน3,00,000 โ โน5,50,000 per year
Actual compensation may vary depending on skills, interview performance, and company policies.
How to Apply
Interested candidates can apply by sending their updated resume to:
๐ง sujith.pirangi@protivitiglobal.in
Candidates who meet the eligibility criteria are encouraged to apply early as pharmacovigilance positions receive high application volume.
You may also share this opportunity with pharmacy graduates seeking drug safety careers