Project Role: Clinical Data Specialist Work Experience: 1.5 - 4 Years

Work location: Homebased Work Mode: Remote Must Have Skills: Clinical data management, Veeva, Startup, Conduct and Closeout.

Job Overview Experience & Background 4–6 years of hands-on Clinical Data Management experience in study start-up, study execution, and closeout activities.

Strong exposure to Veeva EDC is highly preferred.

Experience with eCOA and third-party data reconciliation, and SAE reconciliation (optional but beneficial).

Ability to work independently while effectively collaborating with global teams.

Technical & Functional Skills: Ensure data acquisition, database design, edit check specifications, eCOA integration, and observed dataset requirements aligned with protocol objectives.

Proficiency in tracking, monitoring, and reporting key metrics across study build, execution, and data delivery.

Experience in data validation, discrepancy management, listings review, and QC activities.



Robust understanding of integration of disparate data sources into unified datasets for analytics and decision-making.

Therapeutic knowledge sufficient to perform high-quality data review and identify protocol-relevant trends or issues. Understanding of the technology ecosystem used for clinical data review to ensure accuracy and consistency of database deliverables.

Educational Qualifications: Bachelor's degree OR certification in a related allied health profession from an appropriately accredited institution (i.e. RN, MT, PA, RT).

Minimum of 5 years of data management experience.

Project management experience is required.

Work history at a Clinical Research Organization (CRO) or CRO management experience in data management is required.

Oncology, endocrine and/or inflammatory therapeutic area experience is preferred.

📌 Clinical Data Specialist (India)
🏢 IQVIA India
📍 India