Sr Clinical Data Manager

The Company

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.

Meet the team:

Responsible for data management activities including, but not limited to, developing data management plans, department SOPs, supervising and performing database development, testing, validation, reviewing and processing clinical trial data to ensure the completeness, accuracy, and consistency of clinical trials databases.

Where you come in:

• You will provide input in study protocol design related to data collection and data management.
• You will lead all aspects of data management activities of CRO and external data providers.
• You will ensure that each clinical study database is crafted in accordance with the database definitions outlined in the DMP.
• You will develop study-specific annotated CRFs, database documentation, edit check specifications, data handling conventions, and data entry instructions.
• You will program SAS edit checks and SAS macros for data cleaning.
• You will 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.
• You will coordinate and complete data management activities to meet project timelines.
• You will reconcile device issues, adverse events, and serious events.
• You will maintain 4-5 study databases and data management activities concurrently.
• You will be responsible for filing and maintaining CRFs, …