Description
Liquidia is deeply passionate and committed to the discovery, engineering, and development required to bring novel therapies to patients who need them most, and to the healthcare providers who care for them. Our current drive is toward improving the treatment of pulmonary hypertension (PH). We will continue to combine our proprietary, innovative PRINT® Technology with new and established medications, offering the potential for both better precision and improved clinical outcomes. Our team members include some of the industry’s top scientists, clinicians, business strategists, engineers, and pharmaceutical executives. We work together to help people lead longer, healthier, and happier lives.
The Senior Medical Writer is responsible for the development, writing, editing, and scientific review of high-quality, rigorous Medical Affairs materials supporting YUTREPIA and Liquidia's broader PAH/PH-ILD pipeline (including L606). The role partners closely with Medical Affairs, Clinical Development, HEOR/Market Access, and external medical experts to communicate scientific evidence in a clear, balanced, and compliant manner — with particular emphasis on publications, medical communications, external stakeholder outreach, and congress engagement.
RequirementsRequired:
- 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.
Preferred:
- 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).
Desired Competencies:
- 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.