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 provide input in study protocol design related to data collection and data management.
•    You oversee the data management activities of CRO and external data providers.
•    You ensure that each clinical study database is designed in accordance with the database definitions outlined in the DMP.
•    You develop study-specific annotated CRFs, database documentation, edit check specifications, data handling conventions, and data entry instructions.
•    You program SAS edit checks and SAS macros for data cleaning.
•    You perform all data management activities with no or minimal supervision, including but not limited to database development, testing, validation, site training and support, query resolution, audit, lock, and archive.
•    You coordinate and complete data management activities to meet project timelines.
•    You reconcile device issues, adverse events, and serious adverse events.
•    You maintain 4-5 study databases and data management activities concurrently.
•    You are responsible for filing and maintaining CRFs, subject diaries, and other subject-specific documentation (e.g., Marketing Questionnaires) collected during clinical studies.
•    You are responsible for filing and maintaining digital data (e.g., Dexcom device downloads and blood glucose meter downloads) collected during clinical studies.
•    You write SAS programs to generate tables and listings to facilitate data cleaning.
•    You assist in clinical study CRF-related summary and listing reports using related software.
•    You provide guidance and mentorship to less experienced and/or entry-level Associates of Clinical Data Management.
•    You perform other duties as assigned.

What makes you successful: 

•    You typically require a Bachelor's degree in a technical discipline and a minimum of 5-8 years of related experience, OR a Master's degree with 3-5 years of equivalent industry experience, OR a PhD with 0-2 years of experience. 
•    You have a minimum of 5+ years of related experience in data management or related fields in clinical studies. Your expertise in EDC systems is at a high level. 
•    You are a Certified Clinical Data Manager, with SAS certification and knowledge in SQL or any other programming languages.

What you’ll get: 
•    A front row seat to life changing CGM technology. Learn about our brave #dexcomwarriors community.
•    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. 

#LI-Hybrid
 

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