Medical Writer

Leading document authorship for various clinical projects, the full-time Senior Medical Writer will work remotely, interfacing with clients and supporting larger engagements while leveraging expertise in clinical regulatory writing. Key responsibilities Serve as the project lead on smaller projects and support larger, complex engagements as part of a delivery team Develop submission-level documents and clinical documents such as Clinical Study Reports and Investigator Brochures Interface directly with clients to understand their needs and ensure compliance with regulatory authority guidelines Required qualifications Bachelor''s degree or higher in a scientific discipline strongly preferred 3+ years of regulatory writing experience or equivalent experience with clinical-related documentation Understanding of regulatory authority guidelines and their impact on document creation Experience developing clinical documents, including protocols and submission-level documents Intermediate proficiency with Microsoft Word and document management techniques #J-18808-Ljbffr