Pharmacovigilance Intern
About this internship
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Skills you'll use
What you'll do
- Work on processing adverse-event cases to regulatory standard alongside the core team
- Apply Argus Safety Database, Adverse Event (AE) Reporting, MedDRA Coding, Case Narrative Writing to live, production-facing problems
- Document your work clearly for reviewers and stakeholders
- Participate in reviews and act on the feedback you receive
- Collaborate across engineering, product, design or business as required
- Follow the team's quality, testing and documentation standards
Who can apply
- Pursuing or recently completed B.Pharm/M.Pharm, B.Sc/M.Sc (Life Sciences), BDS, BAMS or MBBS
- Graduating batch 2025, 2026 or 2027 — final-year students and recent graduates welcome
- 60% / 6.0 CGPA and above preferred; strong project work is considered alongside academics
- Working knowledge of Argus Safety Database, Adverse Event (AE) Reporting, MedDRA Coding (or a genuine willingness to learn them)
- Exposure to Case Narrative Writing, Signal Detection Basics, Regulatory Timelines & Compliance is an advantage
- Clear written and verbal communication in English, and care with detail in your work
- No prior work experience required — this is a fresher-friendly internship
- Based in Ahmedabad, Gujarat or willing to work from there for the internship period
Perks & benefits
Interview & selection process
4 rounds — typical selection flow for this role:
- 1Application screening & resume shortlisting by the talent team
- 2Online aptitude / domain assessment
- 3Technical interview on fundamentals and your projects
- 4HR discussion — stipend, start date, expectations and offer
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