Director, Clinical Data Management

Role: Lead study-level clinical data management for oncology trials, overseeing data lifecycle activities, vendor coordination, and cross-functional collaboration. Responsibilities: develop data management plans, oversee CRF design, ensure regulatory compliance, and support data review and cleaning. Collaborate with clinical operations, biostatistics, and external vendors; contribute to protocol and SAP development; lead data review meetings; support process improvements and audits; mentor junior staff as the organization grows. Requirements: Bachelor's degree in life sciences, data sciences, or related; 8+ years of clinical data management experience within biotech, pharma, or CROs; 3+ years managing teams and vendors; strong knowledge of Medidata Rave, CDISC standards, and GCP/ICH guidelines; prior experience supporting oncology trials, especially with complex data types (imaging, genomics) preferred. High-Value: Oncology, biologics or small molecule modalities, clinical trial phases (pre-IND or beyond), vendor oversight, and regulatory support. Work Setup: Hybrid or onsite; no specific travel details provided.