Senior Medical Writer

Date Posted: 2/11/2026

Senior Medical Writer
Remote, NY/NJ

Top Pharmaceutical company in the US is searching for a Contract Medical Writer. This position is representing Medical Writing team at meetings and driving document development discussions.

Position includes the following:
Reviewing CSR-related documents (e.g., Statistical Analysis Plans, TFLs) to ensure content accuracy. Mentoring junior writers and fostering their growth in medical writing. Ensuring adherence to regulatory guidelines, templates, and SOPs for therapeutic area documentation. Contributing to process improvement initiatives across Medical Writing and Global Development teams. Writing and editing clinical documents such as CSRs, protocols, ICFs, narratives, and IBs. Collaborating with clinical teams to articulate document strategies and timelines. Excel at explaining complex medical/scientific concepts to diverse audiences, including lay or patient groups. Thrive in collaborative environments and can foster teamwork to resolve conflicts effectively. Detail-oriented and have a strong ability to manage multiple projects simultaneously. Synthesizing discussions and presenting clear, accurate prose quickly. Committed to adhering to guidelines and standards while continuously improving processes. Mentoring and supporting the development of junior staff members.

Requirements:
Bachelor’s degree (advanced degree preferred). Minimum of 4 years of medical writing experience, including knowledge of clinical research processes. Familiarity with ICH GCP guidelines and proficiency in MS Word, Adobe Acrobat, PowerPoint, and electronic document management systems. Strong organizational and interpersonal skills and experience in clinical document reading, writing, and editing. Pays per hour, rates determined by years of experience.

Please contact Darren Gutowski at dgutowski@clarkdavis.com