Clinical Evaluation Report Medical Writer (1099 Contractor)
Criterion Edge
About this role
Criterion Edge is seeking a remote Medical Writer to collaborate with a team on producing regulatory and scientific documents for clients in the medical device, pharma/biotech, and in vitro device sectors. The role involves supporting high-quality, compliant writing projects, engaging with stakeholders, and maintaining regulatory standards.
Skills
Qualifications
About Criterion Edge
criterionedge.comCriterion Edge is a regulatory writing consultancy that provides best-in-class regulatory writing services for the medical device, biopharma/pharma, and in‑vitro diagnostic industries. They prepare submission‑ready regulatory and clinical documents—such as regulatory submissions, clinical study reports, labeling, and other compliance materials—to help clients meet agency requirements. Branded “The Regulatory Writing Experts,” Criterion Edge combines scientific and regulatory knowledge to improve clarity, consistency, and the efficiency of the approval process. They work with sponsors and manufacturers to translate complex data into clear, compliant regulatory communications.
About Criterion Edge
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Leadership Team
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
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and employee contacts for Criterion Edge.
Salary
$59k – $81k
per year