Biomedical Data Stewardship Manager

A company is looking for a Biomedical Data Stewardship Manager to drive the design, implementation, and governance of standardized data collection practices across clinical programs. Key Responsibilities Design and define standard, indication-level case report form (CRF) libraries and document implementation rules Provide expert consultation and hypercare support to study teams in applying CRF library content Monitor adoption and consistency of CRF standards, conducting audits and reviews to ensure alignment with study and regulatory needs Required Qualifications Doctorate degree or equivalent experience in clinical settings Master's degree with 2 years, Bachelor's degree with 4 years, Associate's degree with 8 years, or High school diploma/GED with 10 years of clinical experience 5+ years of experience in data management, biostatistics, or clinical programming within the pharmaceutical or biotechnology industry Proven experience with CRF design and data standards governance Experience in data collection, analysis, and reporting within drug development and clinical trial processes

Jun 7, 2025 - 00:50
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Biomedical Data Stewardship Manager
A company is looking for a Biomedical Data Stewardship Manager to drive the design, implementation, and governance of standardized data collection practices across clinical programs. Key Responsibilities Design and define standard, indication-level case report form (CRF) libraries and document implementation rules Provide expert consultation and hypercare support to study teams in applying CRF library content Monitor adoption and consistency of CRF standards, conducting audits and reviews to ensure alignment with study and regulatory needs Required Qualifications Doctorate degree or equivalent experience in clinical settings Master's degree with 2 years, Bachelor's degree with 4 years, Associate's degree with 8 years, or High school diploma/GED with 10 years of clinical experience 5+ years of experience in data management, biostatistics, or clinical programming within the pharmaceutical or biotechnology industry Proven experience with CRF design and data standards governance Experience in data collection, analysis, and reporting within drug development and clinical trial processes