Associate Director, Clinical Data Management

Role: Associate Director, Clinical Data Management, overseeing day-to-day management of clinical trial data across relevant phases within an oncology-focused biopharma. Responsibilities: coordinate CDM activities, manage external vendors, ensure data accuracy and completeness, review CRFs, oversee EDC systems, and maintain Data Management Plans. Lead and mentor internal team members, participate in protocol reviews, and ensure compliance with GxP standards. Collaborate closely with CROs, data vendors, and cross-functional teams to support clinical trial success. Requirements: MS, BS/BA or equivalent; 11+ years’ experience designing and executing clinical trials, with strong knowledge of clinical databases, standards, medical coding, ICH, FDA, and GCP guidelines. Demonstrated leadership, teamwork, and industry experience essential. Preferred: oncology experience, especially in solid tumors; 5+ years’ line management. High-value: oncology (solid tumor), clinical trial management, data standards, regulatory compliance, GxP, with a focus on early and late-stage trials. Work setup: not specified; salary range: $186,000–$233,000 USD.