Manager, Data Management Program Lead, Hematology

Role: Program Lead in Data Management overseeing multiple clinical studies or programs, primarily in oncology, from a data perspective. Objectives include ensuring data quality, timeliness, compliance, and process improvement within clinical data management. Responsibilities: lead study teams, manage vendor relationships (CROs, labs), develop and review EDC databases, perform data validation, contribute to protocol and analysis document review, and support process standardization and inspection readiness. May act as the primary data contact and oversee day-to-day data management activities. Requirements: 8+ years of clinical data management experience in biopharma, with at least 5 years in a lead role, strong oncology background, and proficiency in EDC systems like Medidata Rave. Bachelor's degree or equivalent preferred. Skills: project management, cross-functional collaboration, process development, knowledge of ICH/regulatory standards, and proficiency in Microsoft Office and visualization tools. Travel may be required for domestic and international sites. High-value: oncology, clinical trials, data management leadership, EDC systems, regulatory compliance, and process improvement. Work setup: not specified.