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Clinical Data Management

2-5 years
Not Disclosed
10 Dec. 2, 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

Clinical Data Management (CDM) Specialist

Location: Pune, India
Experience: 2–5 Years
Application Deadline: 20-Jan-2026

About the Role

Tata Consultancy Services (TCS) is hiring a Clinical Data Management Specialist to join its growing clinical research team in Pune. The role focuses on ensuring high-quality clinical trial data through meticulous review, reconciliation, and database management. This is an excellent opportunity for life sciences graduates with hands-on experience in Medidata Rave and clinical trial operations.

Key Responsibilities

  • Review and interpret study protocols and adhere to study timelines.

  • Perform data review, reconciliation, and query management, escalating discrepancies as needed.

  • Implement study team feedback and perform external checks to address manual discrepancies.

  • Develop, implement, and test edit checks and listings (DVS).

  • Conduct User Acceptance Testing (UAT) for study databases.

  • Draft and maintain study-specific procedure documents.

  • Ensure accurate, error-free data with all queries resolved.

  • Maintain comprehensive data management study files and documentation.

  • Participate in cross-functional study team meetings, providing updates on data management services.

  • Identify out-of-scope tasks and report to the Team Data Manager (TDM).

  • Assist TDM with study setup activities and provide all study-related reports as requested.

  • Perform Serious Adverse Event (SAE) reconciliation and vendor data reconciliation.

Required Qualifications

  • Bachelor’s or Master’s degree in Life Sciences, Pharmacy, or related fields (B.Pharm, M.Pharm, B.Sc, M.Sc).

Experience and Skills

  • 2–5 years of experience in clinical data management within clinical research studies.

  • Hands-on experience with Medidata Rave.

  • Strong understanding of study setup, conduct, and close-out processes.

  • Proficiency in data review, reconciliation, and query management.

  • Excellent organizational skills, attention to detail, and ability to work in cross-functional teams.

Why Join TCS?

  • Be part of a leading global IT and clinical research organization.

  • Gain exposure to diverse clinical trials and data management processes.

  • Work in a collaborative, fast-paced, and professional environment.