ProPharma 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.
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