Principal Medical Writer

As a Principal Medical Writer you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Responsibilities include developing and authoring clinical and regulatory documents, including clinical study reports, protocols, investigator brochures, and regulatory submissions. Ensuring all documents comply with regulatory guidelines and company standards for quality and accuracy, is key. Collaborating with cross-functional teams, including clinical operations, biostatistics, and regulatory affairs, to gather and interpret clinical data is required. You will also be mentoring and guiding junior medical writers, fostering a culture of excellence and continuous improvement; reviewing and editing documents prepared by other writers to ensure consistency and adherence to regulatory requirements; staying current with industry trends and regulatory changes to integrate best practices into medical writing processes; and contributing to the development of templates, style guides, and standard operating procedures to enhance the efficiency and quality of medical writing activities.