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1-4 years
Not Disclosed
10 Nov. 6, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Company: TCS
Role: Pharmacovigilance – Drug Safety
Work Location: Pune
Experience: 1–4 years of relevant experience in Pharmacovigilance
Job Function: Business Process Services
Role Level: Executive
Job ID: 379417


About the Role

TCS is seeking skilled and detail-oriented professionals for its Pharmacovigilance (PV) Drug Safety team. The ideal candidate will be responsible for performing case processing activities in compliance with global and local regulatory requirements, contributing to patient safety and high-quality deliverables.


Key Responsibilities

  • Perform end-to-end case processing activities, including accessing, coding, and entering safety data in ARGUS.

  • Analyze and interpret complex safety data to ensure accurate and complete case entry.

  • Ensure all case-handling processes comply with global and local pharmacovigilance procedures, regulatory requirements, and internal SOPs.

  • Maintain adherence to Patient Safety objectives, policies, and processes.

  • Collaborate with cross-functional teams to ensure timely delivery of high-quality PV outputs.

  • Support audits, inspections, and continuous improvement initiatives in drug safety operations.


Desired Candidate Profile

Qualifications:

  • Mandatory: B.Pharm / M.Pharm

  • Eligible: BAMS / BHMS / BDS / M.Sc (Biotechnology, Zoology)

Skills & Experience:

  • 1–4 years of hands-on experience in Pharmacovigilance and case processing.

  • Proficiency in ARGUS Safety Database and understanding of case processing workflows.

  • Strong analytical and data interpretation skills.

  • Excellent attention to detail, communication, and documentation abilities.

  • Knowledge of global regulatory requirements for pharmacovigilance.