Senior Medical Writer, Medical Affairs

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Liquidia Corporation

WebsiteLinkedInAlle Stellen

51 - 200 Mitarbeiter

Gegründet 2004

🧬 Biotechnologie

💊 Pharmazie

💰 €75.000.000 Post IPO equity im 2024-02

Biotechnology • Pharmaceuticals

Liquidia ist ein biopharmazeutisches Unternehmen, das sich auf die Entwicklung von inhalierbaren Therapien für seltene kardiopulmonale Erkrankungen spezialisiert hat, insbesondere auf die pulmonal arterielle Hypertonie (PAH) und die mit interstitiellen Lungenerkrankungen assoziierte pulmonale Hypertonie (PH-ILD). Das Unternehmen nutzt seine proprietäre PRINT® Partikeltechnologie, um proprietäre Formulierungen und Verabreichungsmethoden zu entwickeln, die darauf abzielen, die Wirksamkeit, Verträglichkeit und Anwendbarkeit von inhalierbaren Medikamenten zu verbessern; Die Produktpipeline umfasst inhalierbares Treprostinil (kommerzielles Produkt) und klinische Kandidaten wie L606. Liquidia legt besonderen Wert auf Patientenunterstützung, klinische Entwicklung und die Verbesserung von Therapien zur Optimierung von Atemwegsergebnissen.

Beschreibung

• 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.

🎯 Anforderungen

• 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.

🏖️ Vorteile

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