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Job description
MMS Holdings Inc. is a data-focused CRO supporting pharma, biotech, and medical device clients with regulatory submissions and trial data solutions. We seek an experienced Regulatory Medical Writer to lead writing efforts, mentor peers, and ensure quality in a collaborative, ISO-minded environment.
The role emphasizes independent project leadership, client communication, and adherence to 21 CFR Part 11 and GCP standards, shaping strategic deliverables across programs.
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Worksite address
raleigh, NC, 27601, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.