Principal Medical Writer

To support a growing portfolio of clients, the full-time salaried Principal Medical Writer will manage and author clinical program documents, ensuring compliance with regulatory standards while collaborating with cross-functional teams in a remote work environment. Key Responsibilities Independently authors and manages a variety of clinical and regulatory documents, including protocols and study reports Leads cross-functional coordination of resources and manages client expectations, ensuring timely delivery of medical writing projects Supervises and mentors less experienced medical writers, fostering professional development within the team Required Qualifications Bachelor's degree or higher in a medical or scientific discipline Minimum of 7 years of experience in writing clinical and/or regulatory documents for drugs, biologics, or medical devices Advanced knowledge of clinical research principles and regulatory submission requirements Proficiency in MS Word, including experience with tables, graphs, and figures Strong project management skills and ability to work independently with minimal supervision