Senior Medical Writer - Medical Devices & Regulatory

ProPharma Group in the United States seeks an experienced Medical Writer to lead cross-functional projects, author regulatory and clinical documents, and mentor junior writers. The role emphasizes strong communication with clients and internal teams to ensure on-time, compliant deliverables. The candidate should have 7+ years of experience in writing clinical/regulatory documents for drugs, biologics, or devices, and a solid grasp of FDA and ICH guidelines, with hybrid work options and a