01Responsibilities
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.
02Requirements
Pursuing or recently completed B.Pharm/M.Pharm, B.Sc/M.Sc (Life Sciences), BDS, BAMS or MBBS 2026 freshers & final-year students welcome; Working knowledge of Argus Safety Database, Adverse Event (AE) Reporting, MedDRA Coding (or a genuine willingness to learn them); Strong fundamentals in your discipline and clear problem-solving ability; Care with detail and the discipline to document your work; Clear written and verbal communication in English; Based in or willing to work from Kadapa, Andhra Pradesh. .
