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Medical Reviewer

1-3 years
Not Disclosed
10 Nov. 27, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/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

Medical Reviewer

Location: Mumbai, India
Experience Required: 1–3 years
Application Deadline: 14 January 2026
Job Function: Business Process Services
Role: Executive
Job ID: 382817
Industry: Pharmacovigilance / Medical Affairs / Drug Safety
Qualifications: MBBS / MD


About the Role

TCS is hiring a Medical Reviewer to support global pharmacovigilance and drug safety operations. The role involves end-to-end medical review of clinical and post-marketing safety data, ensuring compliance with regulatory standards, and contributing to high-quality safety assessments for marketed and investigational products.


Key Responsibilities

Medical Case Review

  • Conduct medical review of clinical trial cases, spontaneous adverse event reports, solicited reports, and literature-based cases.

  • Perform medical assessment including causality evaluation, labeling assessment, and company causality statement documentation.

  • Review seriousness, coding accuracy, medical relevance, and consistency of safety data.

Safety Data Evaluation

  • Assess case narratives, AE/SAE terms, suspect and concomitant medications, laboratory results, and patient medical history in a global drug-safety context.

  • Ensure completeness, clarity, and scientific accuracy in medical interpretation.

Scientific and Clinical Expertise

  • Maintain up-to-date knowledge of disease biology, therapeutic areas, and key safety concerns for assigned products.

  • Provide medical guidance to drug safety teams on product-related topics and clinical concepts.

Regulatory Compliance

  • Ensure adherence to global and local SOPs, internal timelines, and regulatory requirements.

  • Contribute to inspection readiness and compliance activities.

Cross-Functional Collaboration

  • Represent the safety physician team during internal discussions, client meetings, audits, and safety governance forums.

  • Support quality assurance processes across adverse event data management activities.


Candidate Requirements

Education

  • MBBS or MD (mandatory)

Experience

  • 1 to 3 years of experience in medical review, pharmacovigilance, drug safety, or a related clinical function.

Skills & Competencies

  • Strong understanding of medical terminology, disease mechanisms, and clinical data interpretation.

  • Familiarity with global drug safety regulations and reporting requirements.

  • Ability to analyze safety data with a high level of accuracy and scientific rigor.

  • Strong communication, documentation, and cross-functional collaboration skills.

  • Knowledge of Medical Regulatory processes (preferred).