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 2026, 2027 or 2028 — 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 Bengaluru, Karnataka or willing to work from there for the internship period

Perks & benefits

Interview & selection process

2 rounds — typical selection flow for this role:

1. 1Application screening & resume shortlisting by the talent team
2. 2Discussion with the hiring manager on the role and your fit

About Infomatics

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