Senior Medical Writer

Senior Medical Writer, Publications (Remote, US)

Location: Remote (US-based)

Schedule: Full-Time | Eastern Time hours preferred

EPM Scientific is partnered with a growing medical communications agency seeking a Senior Medical Writer, Publications to support the development of high-impact clinical publications and scientific communications. This is an opportunity to join a highly collaborative team where writers serve as strategic scientific partners and work directly with pharmaceutical clients, investigators, and key stakeholders.

The ideal candidate will have hands-on experience developing Phase III clinical trial manuscripts and a strong ability to translate complex clinical data into compelling, publication-ready scientific narratives.

• Develop, review, and revise peer-reviewed manuscripts, abstracts, posters, congress presentations, slide decks, and related scientific communications.
• Lead the development of clinical trial manuscripts from source materials, including protocols, clinical study reports, statistical outputs, and clinical data.
• Partner directly with clients, authors, investigators, and internal teams to align on scientific messaging, publication strategy, and project timelines.
• Support the development of visual scientific communication materials, including figures, graphical abstracts, posters, and presentations.
• Ensure compliance with publication ethics and industry guidelines, including ICMJE and Good Publication Practice standards.

• PhD, PharmD, or MD
• Minimum of 1 year of medical writing experience within medical communications, pharmaceutical, biotechnology, CRO, or related environments.
• Direct experience serving as an acknowledged medical writer or author on at least one Phase III clinical trial manuscript submitted to a peer-reviewed journal.
• Demonstrated experience developing publications from protocols, CSRs, and other clinical study documentation.
• Strong understanding of clinical research, scientific data interpretation, publication planning, and publication ethics.
• Experience managing publication projects from initiation through submission and/or presentation.

• PhD, PharmD, or MD
• Minimum of 1 year of medical writing experience within medical communications, pharmaceutical, biotechnology, CRO, or related environments.
• Direct experience serving as an acknowledged medical writer or author on at least one Phase III clinical trial manuscript submitted to a peer-reviewed journal.