Clinical Data Analyst 2

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:

The Clinical Data Analyst will be responsible for leading all aspects of data management activities, including developing data automation plans, supervising database development, and ensuring the accuracy, completeness, and consistency pf clinical trial databases through rigorous testing and validation.

Where you come in:

• Automation and System Design - craft and implement automation processes in Clinical Data Management, ensure databases meet established definitions and standards, and conduct independent software development, testing and validation.
• Database Programming and Administration (DBA) - develop and maintain database structures, write and optimize SQL queries, manage database performance, security, and integrity, ensure data integrity and accessibility, and implement data retrieval processes for analysis and reporting.
• SAS Programming - you will program SAS edit checks and macros for data cleaning, develop and implement SAS macros for clinical trials (ETL, validations, analyses, reporting).
• Clinical Data Management - craft Case Report Forms (CRFs) for e-clinical EDC systems, develop annotated CRFs, documentation, edit check specs, and data handling conventions, run over three study databases concurrently.
• Collaboration and Oversight - collaborate on study protocols for data collection and management, coordinate data management tasks with cross-functional teams to meet timelines.
• Documentation and Compliance - you will maintain and file CRFs, …