Clinical Data Management Manager

Role: Lead clinical data management (CDM) activities for Gilead's drug development programs, overseeing data acquisition, analysis, and reporting processes across multiple studies. Responsibilities: design CRF/eCRF, review protocols, oversee vendor data transfers, resolve data queries, ensure data quality and regulatory compliance, and support regulatory submissions and audits. Lead cross-functional collaboration with study teams, investigators, CROs, and vendors; train and mentor staff; participate in process improvements. Qualifications: Bachelor's or Master’s degree with 4-6+ years of CDM or data analytics experience; strong knowledge of FDA/EMA regulations, EDC systems, and clinical trial processes; project management skills and experience leading small projects. Preferred: extensive CDM leadership experience, familiarity with regulatory requirements, and ability to manage complex projects within budget. HighValue: experience supporting late-stage clinical development, regulatory submissions, and working with cross-functional teams in biopharma; role involves vendor oversight, data quality management, and potential travel. WorkSetup: not specified.