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.
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