Sr Medical Affairs Specialist - Regulatory Writing and Scientific Communications
DexcomSan Diego, California, United States
Posted September 29, 2025
95900 - 159900 USD year
Full Time
About the Company
Dexcom Corporation, a leader in glucose sensing technology since 1999, empowers people with diabetes to manage their condition more effectively through continuous glucose monitoring devices. Headquartered in San Diego, Dexcom focuses on developing innovative medical devices and mobile software that provide real-time data and decision support, enabling users to live confidently and pursue their dreams. The company is committed to listening to user needs and continuously improving its products to simplify glucose management worldwide.
Job Description
Dexcom is looking for a Senior Medical Affairs Specialist - Regulatory Writing and Scientific Communications to lead the authoring and updates of Clinical Evaluation Reports (CERs) and related documentation, as well as design and management of compliant literature search strategies. The role requires strong knowledge of EU MDR/MEDDEV expectations for clinical evaluation report and industry regulations and guidelines governing publications and medical communications.
Requirements
- Advanced degree in a relevant scientific field
- Minimum of 3-5 years of experience in regulatory/clinical/medical writing within medical devices, biotech, or pharma
- Strong knowledge of EU MDR/MEDDEV expectations for clinical evaluation report
- Previous experience in diabetes preferred
- Excellent written and verbal communication skills
- Strong project management skills with the ability to manage multiple high-priority projects simultaneously
Benefits
- 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
