Pharmacovigilance Associate
LLRI - Learning Labb Research Institute
Bengaluru, Karnataka, IndiaFresher1d agovia LinkedIn
About the Role
An entry-level Pharmacovigilance Associate to support drug safety monitoring activities, including adverse event case processing and safety database management.
Key Responsibilities
- Process Individual Case Safety Reports (ICSRs) for adverse events
- Perform MedDRA coding of adverse event and medical history terms
- Enter and review safety data in pharmacovigilance/drug safety databases
- Support signal detection and safety data analysis activities
- Assist in preparing periodic safety reports (PSUR/PBRER)
- Ensure compliance with GVP (Good Pharmacovigilance Practices) guidelines
- Support literature screening for safety-relevant information
Qualifications
- B.Pharm/M.Pharm, B.Sc/M.Sc Life Sciences, MBBS, BDS, or PG Diploma in Pharmacovigilance
- Fresher / 0-1 year experience
- Willingness to learn and work in a regulated, compliance-driven environment
Good to Have
- Basic knowledge of MS Office (Word, Excel, PowerPoint)
- Good written and verbal communication skills
- Attention to detail and documentation discipline