Project Data Manager

Role: Lead clinical trial data management for oncology studies, overseeing all aspects from study start-up to database lock, ensuring high-quality deliverables and resource efficiency. Responsibilities include leading data management activities, supervising in-house and CRO/FSP data managers, collaborating with study teams, developing data transfer and eCRF specifications, performing UAT, managing data cleaning and coding, and contributing to study documentation and process improvements. Requirements: 6+ years in clinical data management within the biopharma or biotech industry; proficiency in EDC systems (Medidata Rave preferred), strong project management skills, knowledge of ICH, SDTM/CDASH, and regulatory standards; Bachelor's degree in a health-related field preferred. High-value: oncology, clinical trials, data management, experience with SDTM/CDASH, cross-functional team collaboration, international travel flexibility. Work setup: may involve domestic and international travel; supervisory responsibilities are not specified.