Sr Clinical Data Manager
About the position Dexcom Corporation (NASDAQ DXCM) is a pioneer and global leader in continuous glucose monitoring (CGM). Dexcom began as a small company with a big dream: To forever change how diabetes is managed. To unlock information and insights that drive better health outcomes. Here we are 25 years later, having pioneered an industry. And we're just getting started. We are broadening our vision beyond diabetes to empower people to take control of health. That means personalized, actionable insights aimed at solving important health challenges. To continue what we've started: Improving human health. We are driven by thousands of ambitious, passionate people worldwide who are willing to fight like warriors to earn the trust of our customers by listening, serving with integrity, thinking big, and being dependable. We've already changed millions of lives and we're ready to change millions more. Our future ambition is to become a leading consumer health technology company while continuing to develop solutions for serious health conditions. We'll get there by constantly reinventing unique biosensing-technology experiences. Though we've come a long way from our small company days, our dreams are bigger than ever. The opportunity to improve health on a global scale stands before us. Responsibilities • Provide input in study protocol design related to data collection and data management. • Lead all aspects of data management activities of CRO and external data providers. • Ensure that each clinical study database is crafted in accordance with the database definitions outlined in the DMP. • Develop study-specific annotated CRFs, database documentation, edit check specifications, data handling conventions, and data entry instructions. • Program SAS edit checks and SAS macros for data cleaning. • Perform all data management activities with no or minimal direction, including but not limited to database development, testing, validation, site training and support, query resolution, audit, lock, and archive. • Coordinate and complete data management activities to meet project timelines. • Reconcile device issues, adverse events, and serious events. • Maintain 4-5 study databases and data management activities concurrently. • File and maintain CRFs, subject diaries, and other subject-specific documentation collected during clinical studies. • File and maintain digital data collected during clinical studies. • Write SAS programs to generate tables and listings to facilitate data cleaning. • Assist in clinical study CRF-related summary and listing reports using related software. • Provide guidance and mentorship to junior and/or entry-level Clinical Data Management associates. • Other duties as assigned. Requirements • Minimum of 5+ years of related experience in data management or related fields in clinical studies. • High level of expertise in EDC systems. • Certified Clinical Data Manager, SAS certification, knowledge in SQL or any other programming languages. • Typically requires a Bachelor's degree in a technical discipline, and a minimum of 5-8 years related experience or a Master's degree and 2-5 years equivalent industry experience or a PhD and 0-2 years experience. Benefits • A front-row seat to life-changing CGM technology. • A full and comprehensive benefits program. • Growth opportunities on a global scale. • Access to career development through in-house learning programs and/or qualified tuition reimbursement. • An exciting and innovative, industry-leading organization committed to our employees, customers, and the communities we serve. Apply tot his job