Principal Medical Writer

Leading the development of high-quality regulatory and clinical documents, the full-time Principal Medical Writer will oversee medical writing workstreams, collaborate with cross-functional teams, and mentor junior writers in a remote setting. Key responsibilities Lead the preparation and review of clinical study reports, protocols, and other regulatory documents to ensure accuracy and clarity Collaborate with clinical research, biostatistics, and regulatory affairs teams to gather and synthesize information for document development Provide guidance on best practices for medical writing and mentor junior medical writers to foster professional growth Required qualifications A bachelor's degree in life sciences, pharmacy, or a related discipline Significant experience in medical writing, particularly in regulatory submissions and clinical documentation Strong understanding of regulatory requirements and industry standards for clinical writing Exceptional writing and editing skills, with a keen eye for detail and clarity Excellent communication and interpersonal skills for effective collaboration with diverse teams Experience: 3 years required