Navitas Life Sciences has announced recruitment for the position of Drug Safety Associate in Bangalore, India. This opportunity is ideal for professionals with 1–5 years of pharmacovigilance (PV) or drug safety experience who are looking to advance their careers in case processing, safety data management, and regulatory compliance within the pharmaceutical and life sciences industry.
Candidates with relevant experience in Individual Case Safety Report (ICSR) processing, Argus Safety, MedDRA coding, pharmacovigilance regulations, and global drug safety operations are encouraged to apply.
Job Overview
| Particular | Details |
|---|---|
| Company | Navitas Life Sciences |
| Job Role | Drug Safety Associate |
| Experience | 1–5 Years |
| Job Location | Bangalore, Karnataka, India |
| Employment Type | Full Time |
| Department | Pharmacovigilance / Drug Safety |
| Salary (Estimated) | ₹4.5–8.5 LPA |
| Last Date | Apply as early as possible |
Key Responsibilities
As a Drug Safety Associate at Navitas Life Sciences, selected candidates may be responsible for:
- Processing Individual Case Safety Reports (ICSRs) from multiple sources.
- Reviewing adverse event reports for completeness, consistency, and regulatory compliance.
- Performing medical coding using MedDRA and WHO Drug Dictionary where applicable.
- Maintaining accurate pharmacovigilance documentation and case records.
- Ensuring compliance with global pharmacovigilance regulations, SOPs, and quality standards.
- Supporting case follow-up activities and reconciliation processes.
- Working with global safety teams to meet regulatory submission timelines.
- Contributing to quality improvement initiatives and audit readiness.
Qualifications
Candidates with the following educational backgrounds are generally suitable:
- B.Pharm, M.Pharm, Pharm.D, BDS, MBBS, B.Sc Nursing, M.Sc Life Sciences, Biotechnology, Microbiology, Biochemistry, Zoology, or other relevant Life Sciences degrees.
Preferred Skills
Applicants with the following skills will have an advantage:
- Pharmacovigilance and Drug Safety knowledge
- Individual Case Safety Report (ICSR) processing
- Argus Safety or other safety databases
- MedDRA coding
- WHO Drug Dictionary
- Good Documentation Practices (GDP)
- Regulatory compliance (ICH-GCP, GVP)
- Attention to detail
- Effective communication skills
- Ability to work in cross-functional teams
Why Join Navitas Life Sciences?
Working with Navitas Life Sciences offers professionals an opportunity to:
- Build a career in global pharmacovigilance.
- Gain exposure to international pharmaceutical clients.
- Work with advanced drug safety technologies and workflows.
- Learn from experienced pharmacovigilance professionals.
- Access career development and continuous learning opportunities.
- Work in a collaborative life sciences environment.
How to Apply
Interested candidates who meet the eligibility criteria can share their updated resume via email:
Email: recruitment.bangalore@navitaslifesciences.com
Apply at the earliest, as applications are reviewed on a rolling basis.