Clinical Data Validation Associate

Job Role: Clinical Data Validation Associate
Experience: 5+ Years
Location: Pan India (Remote)

Job Description:

We are seeking a highly motivated and detail-oriented Clinical Data Programmer / Clinical Data Review Specialist to support clinical trial data review, visualization, and reporting activities. The ideal candidate will possess strong knowledge of the drug development process, clinical data standards, and regulatory requirements, along with hands-on experience in programming clinical data listings, visualizations, and reports using industry-standard tools.

Key Responsibilities

• Develop, maintain, and validate clinical data listings, reports, dashboards, and visualizations for clinical studies.
• Perform ongoing clinical data review and support data cleaning activities throughout the clinical trial lifecycle.
• Utilize tools such as Veeva CDB, JReview, and Elluminate to support data review and reporting requirements.
• Design and develop custom reports and visualizations in Elluminate.
• Collaborate with Clinical Data Management, Biostatistics, Statistical Programming, and Clinical Operations teams to identify and resolve data issues.
• Ensure compliance with regulatory requirements and industry data standards, including CDISC and SDTM.
• Generate ad hoc reports and listings to support study teams, safety reviews, and regulatory submissions.
• Review and interpret data discrepancies, trends, and anomalies within clinical databases.
• Support database lock activities and data quality review processes.
• Create and maintain programming documentation, specifications, and validation records.

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