Senior Medical Writer, Medical Affairs

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Liquidia Corporation

WebsiteLinkedInAll Job Openings

51 - 200 employees

Founded 2004

🧬 Biotechnology

💊 Pharmaceuticals

💰 $75M Post IPO equity on 2024-02

Biotechnology • Pharmaceuticals

Liquidia is a biopharmaceutical company focused on developing inhaled therapies for rare cardiopulmonary diseases, particularly pulmonary arterial hypertension (PAH) and pulmonary hypertension associated with interstitial lung disease (PH-ILD). The company leverages its proprietary PRINT® particle engineering technology to create proprietary formulations and delivery methods aimed at improving efficacy, tolerability, and convenience of inhaled medicines; its pipeline includes inhaled treprostinil (commercial product) and clinical-stage candidates such as L606. Liquidia emphasizes patient support, clinical development, and advancing therapies for improved respiratory outcomes.

📋 Description

• 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. • Support the medical review process for promotional and non-promotional materials as needed. • 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.

🎯 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. • Demonstrated end-to-end publication management experience (GPP 2022/ICMJE fluency required). • 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. • Familiarity with AMA style, medical review committee (MRC) processes, and publication/medical communication tools (e.g., EndNote, Veeva Vault). • Exceptional scientific writing and editing with strong attention to accuracy and balance. • Ability to translate complex clinical/scientific data for varied audiences. • Strong project management skills; able to manage multiple concurrent projects against tight congress/publication deadlines. • Effective cross-functional and stakeholder management, including with external authors and vendors. • Working understanding of evidence generation and dissemination strategy.

🏖️ Benefits

• Medical • Dental • Vision • STD • LTD • 401(k) Savings Retirement Plan • ESPP • and more!