Job Description
Join BMS in Uxbridge as an Associate Director of Clinical Data Management. Influence clinical development programs and lead data quality initiatives within the biopharma sector.
In this pivotal role at BMS, you will coordinate clinical data management for high-impact development programs. You will set industry-leading data standards, mentor junior leads, and represent your team at regulatory submissions. Your hands-on experience with EDC systems and strong grasp of FDA guidelines will set you apart in this position.
Key Responsibilities:
• Own and manage data processes across clinical development programs
• Define program-level data standards alongside global teams
• Conduct Data Quality Review meetings for trial data oversight
• Mentor junior leads to foster talent in the field
• Collaborate with cross-functional teams for regulatory submissions
Requirements:
• 7+ years in biopharma or CRO environments, 3+ in leadership
• Deep knowledge of FDA/ICH guideli...
In this pivotal role at BMS, you will coordinate clinical data management for high-impact development programs. You will set industry-leading data standards, mentor junior leads, and represent your team at regulatory submissions. Your hands-on experience with EDC systems and strong grasp of FDA guidelines will set you apart in this position.
Key Responsibilities:
• Own and manage data processes across clinical development programs
• Define program-level data standards alongside global teams
• Conduct Data Quality Review meetings for trial data oversight
• Mentor junior leads to foster talent in the field
• Collaborate with cross-functional teams for regulatory submissions
Requirements:
• 7+ years in biopharma or CRO environments, 3+ in leadership
• Deep knowledge of FDA/ICH guideli...
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