Senior Medical Writer, Medical Affairs

This is a fully remote position, open to applicants in United States.

📋 Description

• Create manuscripts, review articles, congress abstracts, posters, and oral presentations related to the PAH/PH-ILD portfolio.

• Assist in the formulation of the publication plan and timeline in collaboration with the publications lead, ensuring alignment with data readouts, congress schedules, and cross-functional review processes.

• Oversee publication vendors, coordinate reviews from authors and steering committees, and maintain the publication tracking database.

• Ensure adherence to Good Publication Practice (GPP 2022) and ICMJE authorship standards at all stages.

• Aid in the development of core scientific platforms, disease-state educational materials, clinical data presentations, and product scientific narrative documents.

• Create and maintain the MSL slide library, MSL training resources, FAQs, and scientific response letters.

• Assist in the medical review process for both promotional and non-promotional materials as required.

• Convert complex clinical and scientific data into clear and balanced content for healthcare professionals, payers, and internal stakeholders.

• Support the creation and upkeep of Standard Response Letters and literature/scientific digests.

• Facilitate responses to unsolicited scientific inquiries and ensure the Medical Information reference library is up-to-date.

• Contribute to engagement with KOLs, advocacy groups, and professional societies by producing scientifically accurate written content.

• Collaborate with Advocacy and Field Medical to guarantee materials reflect current data and assist in relationship-building goals.

• Develop materials for advisory boards, investigator meeting presentations, and post-meeting scientific summaries.

• Assist in the development of scientific content for congress activities, including abstracts, posters, symposia materials, and booth/exhibit scientific content.

• Support pre- and post-congress initiatives, including competitive intelligence summaries and internal debrief documents.

• Ensure content development aligns with Liquidia's tiered Congress Strategy framework and KOL engagement standards.

• Collaborate with Medical Directors, Field Medical, Clinical Innovation & Strategic Engagement, HEOR/Market Access, Regulatory, and Legal/Compliance to guarantee scientific accuracy, balance, and regulatory compliance across all materials.

• Coordinate with the Commercial team on non-promotional reviews as necessary.

⛳️ Requirements

• Advanced scientific degree preferred (PharmD, PhD, MD, or MS in Life Sciences); strong candidates with a BS and substantial relevant writing experience will also be considered.

• Significant experience in pharmaceutical medical writing, ideally with direct Medical Affairs involvement.

• Proven end-to-end publication management experience (GPP 2022/ICMJE fluency required).

• A strong history of developing congress abstracts, posters, and scientific presentations.

• Excellent scientific writing, editing, and communication abilities.

• Experience in pulmonary hypertension, rare diseases, respiratory conditions, or orphan drugs.

• Familiarity with AMA style, medical review committee (MRC) processes, and publication/medical communication tools (e.g., EndNote, Veeva Vault).

• Exceptional scientific writing and editing skills with a keen focus on accuracy and balance.

• Capability to translate complex clinical and scientific data for diverse audiences.

• Strong project management skills; capable of managing multiple concurrent projects under tight congress/publication deadlines.

• Effective cross-functional and stakeholder management, including collaboration with external authors and vendors.

• Working knowledge of evidence generation and dissemination strategies.

🏝️ Benefits

• Medical

• Dental

• Vision

• STD

• LTD

• 401(k) Savings Retirement Plan

• ESPP

• and more!