Associate Director, Clinical Data Management

Role: Associate Director of Clinical Data Management at Bristol Myers Squibb, overseeing end-to-end data activities for complex clinical trials within the R&D pipeline. Responsibilities include leading data collection strategies, managing vendors, ensuring data quality, authoring study-related plans, and supporting audits and inspections. The role involves collaborating with cross-functional teams, setting data standards, and driving continuous improvement initiatives. Requirements: Bachelor's in life sciences, data science, or related field; 7+ years experience in biopharma/CRO, with 3+ years in a leadership role; strong knowledge of clinical data management, GxP, FDA/ICH guidelines, and EDC systems (preferably Medidata RAVE); excellent project management and communication skills. Preferred qualifications include advanced degrees and experience supporting clinical trials, especially in biologics or cell therapy modalities, with involvement in regulatory submissions. High-value specifics: leadership of complex clinical data projects, vendor oversight, compliance with industry standards, and cross-functional interface with study teams, vendors, and regulatory bodies. Work setup: hybrid onsite depending on role structure, with some travel (5-10%) for industry events and inspections.