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Associate Director, Clinical Data Management Trial Lead

Merck • Rahway, NJ, US • published 2026-10-09 15:03:12.477729

Description

Job Description Under the direction of Therapeutic Area (TA) leadership, the CDM (Clinical Data Management) Trial Lead is accountable for end\-to\-end delivery of data management activities for assigned studies, ensuring quality, integrity, and compliance with GDMS standards and regulatory requirements. The role provides strategic and operational oversight across the trial lifecycle, serves as the primary data management contact for cross\-functional teams, and contributes to process improvement and capability development within the global GDMS community. **Responsibilities:** * Lead end\-to\-end clinical data management activities for assigned studies from study start\-up through database lock and archival in accordance with defined processes, timelines, quality targets, Standard Operating Procedures (SOPs), International Council for Harmonization – Good Clinical Practice (ICH\-GCP), and protocol\-specific requirements; partner with assigned leadership for alignment on strategy, risks, and escalations. * Oversee clinical data collection design and review across all data types—defined as reconciliation, logical consistency review, and remediation of study data from multiple sources...

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