Key Responsibilities

- Perform clinical data management activities, including data cleaning, manual and system checks, and updating relevant trackers.
- Manage data discrepancies, clinical queries, and issues, ensuring timely resolution and data accuracy.
- Support database lock activities and ensure all required tasks are completed within agreed timelines.
- Identify activities at risk of missing client SLAs and develop corrective action plans in coordination with the Team Lead (TL).
- Maintain and archive essential study documentation and records in accordance with audit, quality, and information security requirements.
- Ensure reliable and timely retrieval of clinical trial documentation and information for audit purposes.
- Support multiple clinical trials across diverse therapeutic areas and contribute to their successful completion.




- Provide technical oversight and operational support for clinical data management activities whenever required.
- Work with clinical data systems such as Medidata Rave and Veeva EDC.
- Handle third-party vendor data, including laboratory, pharmacokinetic (PK), imaging, and other external clinical data.
- Use Spotfire reporting tools for data review, tracking, and reporting activities.
- Communicate effectively with clients and internal stakeholders to provide updates, resolve queries, and ensure smooth study delivery.

Valuable-to-Have Skills

Spotfire Reporting, Multiple Therapeutic Area Experience, Technical Oversight, Clinical Data Reporting, Vendor Data Reconciliation, Clinical Data Standards, Process Improvement.

📌 SPE-Clinical Data Management (India)
🏢 Cognizant Technology Solutions India
📍 India