Sr. Medical Writer, Medical Affairs

Job Responsibilities

• Draft manuscripts, review articles, congress abstracts, posters, and oral presentations across the PAH/PH-ILD portfolio.
• Support the development of the publication plan and timeline in coordination with the publications lead, ensuring alignment with data readouts, congress calendars, and cross-functional review cycles.
• Manage publication vendors, coordinate author and steering committee reviews, and maintain the publication tracking database.
• Ensure compliance with Good Publication Practice (GPP 2022) and ICMJE authorship standards throughout.
• Support the development of the core scientific platform, disease-state education materials, clinical data decks, and product scientific narrative documents.
• Build and maintain the MSL slide library, MSL training materials, FAQs, and scientific response letters.
• Translate complex clinical and scientific data into clear, scientifically balanced content for HCP, payer, and internal audiences.
• Support the development and maintenance of Standard Response Letters and literature/scientific digests.
• Support responses to unsolicited scientific inquiries and keep the Medical Information reference library current.
• Support engagement with KOLs, advocacy organizations, and professional societies through scientifically accurate written content.
• Partner with Advocacy and Field Medical to ensure materials reflect current data and support relationship-building objectives.
• Develop advisory board materials, investigator meeting presentations, and post-meeting scientific summaries.
• Support scientific content development for congress activities: abstracts, posters, symposia materials, and booth/exhibit scientific content.
• Support pre- and post-congress activity, including competitive intelligence summaries and internal debrief materials.
• Align content development with Liquidia's tiered Congress Strategy framework and KOL engagement standards.
• Partner with Medical Directors, Field Medical, Clinical Innovation & Strategic Engagement, HEOR/Market Access, Regulatory, and Legal/Compliance to ensure scientific accuracy, balance, and regulatory compliance across all deliverables.
• Coordinate with Commercial on non-promotional review as needed.

Job Requirements

• Advanced scientific degree preferred (PharmD, PhD, MD, or MS in Life Sciences); strong candidates with a BS and significant relevant writing experience will also be considered.
• Meaningful pharmaceutical medical writing experience, ideally including direct Medical Affairs experience.
• Strong track record developing congress abstracts, posters, and scientific presentations.
• Excellent scientific writing, editing, and communication skills.
• Pulmonary hypertension, rare disease, respiratory, or orphan drug experience (preferred).
• Familiarity with AMA style, medical review committee (MRC) processes, and publication/medical communication tools (e.g., EndNote, Veeva Vault) (preferred).