Medical Information Manager

🕒 il y a 3 jours

🌲 North Carolina – Distant

🌲 North Carolina – Remote

⏰ Temps Plein

🟡 Intermédiaire

🟠 Senior

👔 Manager

👻 Score fantôme 10%

Ce que ça veut dire : la probabilité que cette offre reste ouverte sans recrutement actif.Comment le lire : 60 % ou plus, on pense que c'est une offre fantôme. Un score plus bas est moins inquiétant.Comment on la calcule : ancienneté, republications, postes ouverts vs taille de l'équipe, rapidité de clôture, et si le salaire est indiqué.À noter : une estimation à partir de données publiques, pas un jugement sur l'entreprise. De vraies offres peuvent avoir un score élevé, alors prenez-le comme un indice, pas comme un fait.

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Liquidia Corporation

Site WebLinkedInTous les Emplois

51 - 200 employés

Fondée en 2004

🧬 Biotechnologie

💊 Pharmaceutique

💰 €75 000 000 Post IPO equity en 2024-02

Biotechnology • Pharmaceuticals

Liquidia est une entreprise biopharmaceutique se concentrant sur le développement de thérapies inhalées pour les maladies cardiopulmonaires rares, en particulier l'hypertension artérielle pulmonaire (HTAP) et l'hypertension pulmonaire associée à une maladie pulmonaire interstitielle (HP-MPI). La société s'appuie sur sa technologie propriétaire d'ingénierie de particules PRINT® pour créer des formulations et des méthodes de livraison exclusives visant à améliorer l'efficacité, la tolérance et la commodité des médicaments inhalés ; son portefeuille comprend le trépostinil inhalé (produit commercial) et des candidats en phase clinique comme le L606. Liquidia met l'accent sur le soutien aux patients, le développement clinique et la progression des thérapies pour de meilleurs résultats respiratoires.

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

🎯 Exigences

• 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

🏖️ Avantages

• 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