Manager, Submission Management, Clinical Trials
Central London, London, United Kingdom
Bristol-Myers Squibb Co
compliance with study timelines, BMS SOPs, worldwide regulatory guidelines and regulations. Comply with the use and maintenance of the available planning & tracking tools (e.g. Veeva - HA submission and approval Tracking system) to generate reports and track the CTA content and associated dates. Escalate to study teams and GSM-CT more ยป
Employment Type: Permanent
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