Senior Clinical Data Manager

📋 Description

• • The Senior Clinical Data Manager is responsible for managing all aspects of the clinical trial data management process from study start-up to post-database lock for assigned projects, ensuring compliance with SOPs, regulatory directives, and study-specific plans.
• • Day-to-day responsibilities include serving as the primary data management contact for clinical projects, overseeing data entry processes and quality control, developing CRF specifications, conducting database build UAT, managing timelines and resources, performing medical coding, coordinating SAE/AE reconciliation, liaising with third-party vendors, and providing leadership on cross-functional initiatives.
• • Precision Medicine Group is a specialized CRO that integrates clinical trial execution with deep scientific knowledge, laboratory expertise, and advanced data sciences to improve the speed, cost, and success rate of bringing life-changing therapies to patients, with a growing presence in the Asia Pacific region.
• • The role offers opportunities to develop leadership skills, deepen expertise in clinical data management systems (e.g., Medidata Rave, Veeva), contribute to SOP development, gain exposure to therapeutic areas like oncology and orphan drugs, and influence data quality and trial success across global projects.