Medical Information Manager

🔥 4 minutes ago

🌲 North Carolina – Remote

🌲 North Carolina – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

👔 Manager

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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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

• Respond to verbal and written medical inquiries from internal and external customers about post-launch products • Author medical information letters, dossiers, documents, and presentations • Disseminate current, accurate, fair-balanced scientific and medical information • Support capture and reporting of adverse events and product complaints while maintaining compliance • Develop and update data-driven responses to customer inquiries • Communicate information promptly to internal and external customers • Collaborate with Pharmacovigilance, Quality, Field Medical, Medical Affairs, Regulatory, Marketing, and Commercial teams • Proofread and edit medical content for grammatical accuracy, clarity, and consistency • Review medical and promotional content through the Medical, Legal, and Regulatory process in Veeva systems • Perform medical accuracy reviews of promotional materials • Ensure content complies with regulatory and company standards • Track reviewer feedback and implement revisions • Develop, organize, and maintain repositories of standard medical responses, FAQs, and reference materials • Update resources based on new evidence, product updates, and regulatory guidance • Provide approved medical content to Medical Affairs and cross-functional teams • Monitor key publications and share concise scientific summaries • Ensure communications comply with regulatory requirements and ethical standards • Stay current on industry guidelines and best practices • Provide off-hours support for urgent medical inquiries • Represent Medical Affairs at scientific congresses through booth engagements • Manage the RightFind copyright clearinghouse and EndNote publication library

🎯 Requirements

• 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 • 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 for medical response letters, scientific summaries, and HCP-facing content • Familiarity with the Medical, Legal, and Regulatory review process and standards for promotional and scientific materials • Ability to partner across Medical Affairs, Regulatory, Marketing, and Commercial teams • Strong influencing, facilitation, and presentation abilities • Ability to serve 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 • Preferred: 1+ years of medical writing experience • Preferred: Participation in accredited medical writing associations is a plus • Preferred: Experience with IRMS or Veeva MI as a user and administrator, or technical proficiency to learn quickly • Preferred: Experience with publication review • Preferred: Clinical experience in pulmonary hypertension

🏖️ Benefits

• Competitive compensation package • Medical insurance • Dental insurance • Vision insurance • Short-term disability (STD) • Long-term disability (LTD) • 401(k) Savings Retirement Plan • Employee Stock Purchase Plan (ESPP) • Reasonable accommodation for qualified individuals with disabilities