Navitas Life Sciences is a leading global provider of drug development, regulatory, and pharmacovigilance solutions. With expertise in clinical research, regulatory submissions, and safety monitoring, Navitas helps pharmaceutical companies bring safer drugs to market.
📍 Location: Bangalore (Whitefield)
💼 Work Mode: WFO/Hybrid
🎓 Education: M.Pharm / B.Pharm / Pharm.D
📅 Experience: 1-3 years
Job Description: Safety Associate (Aggregate)
Key Responsibilities:
✔ Review and authorize DSUR, PBRER, PADER, PSUR reports
✔ Ensure compliance with GCP, GVP, ICH, and USFDA guidelines
✔ Perform aggregate safety data analysis and risk management
✔ Collaborate with cross-functional teams for pharmacovigilance activities
✔ Maintain high-quality documentation and reporting standards
Required Skills & Eligibility:
✅ Education: M.Pharm / B.Pharm / Pharm.D
✅ Experience: 1-3 years in aggregate reporting (DSUR, PBRER, PSUR)
✅ Strong knowledge of GCP, GVP, ICH, and FDA regulations
✅ Excellent analytical and communication skills
Why Join Navitas Life Sciences?
Benefits & Perks:
🔹 Competitive salary & growth opportunities
🔹 Hybrid work model (WFO + Flexibility)
🔹 Learning & development programs
🔹 Collaborative work environment
How to Apply?
📩 Email your CV to: varsha.mane@navitaslifesciences.com
📌 Subject Line: “Aggregate Role”
🚀 Don’t miss this opportunity! Apply today!
