Medical Information Manager

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.

Location: This position may be performed remotely but requires flexibility and willingness to travel as needed.

Liquidia Technologies seeks a dedicated and detail-oriented Medical Information Manager to join our dynamic Research Triangle Park (RTP), NC team. As a key contributor to our Medical Affairs department, you will be crucial in authoring and disseminating accurate, current, and fair-balanced scientific and medical information. Your expertise will help ensure that healthcare professionals and patients receive timely and reliable information, ultimately enhancing patient outcomes.

In this role, you will own the development and maintenance of standard medical response documents and the company’s medical information repository, ensuring healthcare professionals, patients, and internal partners receive timely, evidence-based responses to medical inquiries about Liquidia’s products. Provide off-hours support for urgent medical inquiries and represent Medical Affairs at scientific congresses through booth engagements.

This role also supports the Medical, Legal, and Regulatory (MLR) review of promotional and scientific materials and contributes to Medical Education initiatives. You will serve as the primary lead for Medical in the Publication Review Committee (PRC), overseeing the review and approval of scientific publications and promotional materials to ensure accuracy and compliance. The Medical Information Manager safeguards scientific and regulatory integrity across all communications while helping Medical Affairs serve as a trusted resource across the organization.

The ability to synthesize complex data and communicate effectively will be essential in supporting our mission to develop innovative therapies for rare and life-threatening diseases.

This role will also monitor scientific literature and communicate new data to relevant internal groups. This role will develop, organize, and maintain the company’s repository of standard medical responses, FAQs, and reference materials. Management of the copyright clearinghouse, Right Find, and publication library, Endnote, is necessary to communicate and house relevant information.

• Doctor of Pharmacy (PharmD) with an active pharmacy license or completion of a Residency or Fellowship in Medical Information.
• Minimum 3-5 years of pharmaceutical industry/medical information experience.
• Experience in abstracting databases (Embase and Pub Med) for literature searches and full-text document retrieval.
• Ability to manage multiple projects, prioritize effectively, and deliver under tight timelines. Awareness of regulations and guidelines related to Medical Information and Medical Affairs.
• Strong writing and editing skills to prepare medical response letters, scientific summaries, and HCP-facing content with accuracy and clarity.
• Familiarity with the Medical, Legal, and Regulatory review process and standards for promotional and scientific materials.
• Proven ability to partner effectively across Medical Affairs, Regulatory, Marketing, and Commercial teams to align…