[Hiring] Medical Information Manager @Liquidia

Role Description

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.

• Own the development and maintenance of standard medical response documents and the company’s medical information repository.
• Ensure 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.
• Represent Medical Affairs at scientific congresses through booth engagements.
• Support the Medical, Legal, and Regulatory (MLR) review of promotional and scientific materials.
• Contribute to Medical Education initiatives.
• 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.
• Safeguard scientific and regulatory integrity across all communications.
• Monitor scientific literature and communicate new data to relevant internal groups.
• Develop, organize, and maintain the company’s repository of standard medical responses, FAQs, and reference materials.
• Manage the copyright clearinghouse, RightFind, and publication library, Endnote.

Qualifications

• 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 PubMed) for literature searches and full-text document retrieval.
• 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 messaging and ensure compliance.
• Strong influencing, facilitation, and presentation abilities; capable of serving as a medical information subject matter expert internally and externally.
• Self-motivated and eager to learn new skills.
• Demonstrated ability to work cross-functionally.
• Up to 15% domestic travel required.

Requirements

• 1+ years of medical writing experience (preferred).
• Participation in accredited medical writing associations (e.g., American Medical Writers Association) is a plus.
• Experience with IRMS – Information Request Management System or Veeva MI as a user and administrator, or technical proficiency with the ability to quickly learn.
• Experience with publication review.
• Clinical experience in pulmonary hypertension.