Senior Medical Writer—Regulatory & Clinical Solutions
Listed on 2026-10-11
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Healthcare
Medical Science Liaison, Healthcare Compliance, Clinical Research
Pro Pharma is seeking a Principal Medical Writer to author and edit high-quality medical writing deliverables across clinical, safety, and regulatory areas. You will collaborate with cross-functional teams, manage timelines, and mentor junior writers in a hybrid, client-focused environment.
The role requires a Bachelor’s degree in a medical or scientific field and a minimum of 7 years in writing clinical or regulatory documents for drugs, biologics, devices, or diagnostics.
The Senior Medical Writer—Regulatory & Clinical Solutions role at Pro Pharma is now open for applications in Raleigh, NC, United States.
The advertised compensation is 110..
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Senior Medical Writer—Regulatory & Clinical Solutions role in the description above.
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