Global Regulatory Partners
The Clinical Evaluation Report (CER) Writer is responsible for creating regulatory submission documents related to Clinical Evaluation Reports (CERs) for the medical device industry. This position involves client interaction, mentoring other writers, and ensuring compliance with EU regulations and internal standards. The role requires synthesizing complex clinical data and managing multiple projects in a fully remote capacity.
Headquarters
Framingham, Massachusetts, United States
We are a consulting company that provides a full spectrum of Market Access services that includes tailored solutions for our clients
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
View leadership team, funding history,
and employee contacts for Global Regulatory Partners.
Global Regulatory Partners didn’t post a salary, so this is our estimate from similar listings.
27% below the average for this role