Founded in 1999, Dexcom, Inc. (NASDAQ: DXCM), is developing and marketing Continuous Glucose Monitoring (CGM) systems for ambulatory use by people with diabetes and by healthcare providers for the treatment of people with diabetes. The company is the leader in transforming diabetes care and management by providing CGM technology to help patients and healthcare professionals better manage diabetes. Since the company’s inception, Dexcom has focused on better outcomes for patients, caregivers, and clinicians by delivering solutions that are best in class—while empowering the community to take control of diabetes. Headquartered in San Diego, California, with additional offices in the U.S., Europe, and Asia Pacific, the company employs over 8,000 people globally.

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, advers 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. Marking 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 will have other duties as assigned.

What Makes You Successful

• You have minimum 5 years related experience in data management or related fields in clinical studies.
• You have a high level of expertise in EDC systems.
• You are a Certified Clinical Data Manager, SAS certification, 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.

Travel Required

• 15 - 25%

Experience And Education

• Typically requires a Bachelors degree in a technical discipline, and a minimum of 5-8 years related experience or Masters degree and 2-5 years equivalent industry experience or a PhD and 0-2 years experience.