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Director, Publication Strategy – Execution

🕒 vor 13 Tagen

🌲 North Carolina – Remote

infoinfo

⏰ Vollzeit

🔴 Experte

👔 Direktor

🗣️🇺🇸🇬🇧 Englisch erforderlich

Woher diese Stelle stammt

Veröffentlicht auf der Karriereseite von BioCryst Pharmaceuticals, Inc., nicht über eine Jobbörse

Von Remote Rocketship zum ersten Mal gesehen vor 13 Tagen

Noch offen auf der Website von BioCryst Pharmaceuticals, Inc.. Geprüft vor 39 Minuten.

Logo of BioCryst Pharmaceuticals, Inc.

BioCryst Pharmaceuticals, Inc.

501 - 1000 Mitarbeiter

🏥 Gesundheitswesen

💼 Beratung

📦 Logistik

💰 €450.000.000 Post-IPO Debt - BioCryst Pharmaceuticals im 2023-04

Healthcare • Consulting • Logistics

BioCryst Pharmaceuticals, Inc. ist ein global tätiges Biotechnologieunternehmen, das sich auf die Entdeckung, Entwicklung und Vermarktung neuartiger oraler kleiner Moleküle und Proteintherapeutika für seltene Krankheiten, insbesondere hereditäres Angioödem (HAE), konzentriert. Seit seiner Gründung im Jahr 1986 nutzt BioCryst strukturgeleitetes Wirkstoffdesign, medizinische Chemie und fortschrittliche Technologien, um erstklassige oder best-in-class Medikamente zu entwickeln, und arbeitet eng mit Patienten, Interessengruppen und globalen Partnern zusammen, um Behandlungen auf den Markt zu bringen.

Beschreibung

• Serve as the subject matter expert on publication-related matters • Ensure relevant data, analysis, interpretation, communication, and publication planning • Adhere to good publications practices and BioCryst policies • Develop and revise internal guidance and policies supporting publication activities • Deliver training to internal cross-functional teams and external partners • Lead development and execution of medical and scientific publications across the hereditary angioedema and pipeline portfolio • Coordinate resources and, when needed, execute abstracts, posters, oral presentations, manuscripts, and scientific/medical meeting presentations • Coordinate writing, editing, formatting, and submission of articles to peer-reviewed journals and scientific/medical conferences • Build and maintain relationships with clinical experts, journal editors, and congress personnel • Manage annual budget, work, resource allocation, contracts, SOWs, and invoices • Manage publication vendors day to day • Oversee publication-planning platform documents for completeness, accuracy, and integrity • Keep current with GPP and ISMPP standards

🎯 Anforderungen

• Advanced scientific degree required (PharmD, PhD, MD/DO) • Minimum 10 years of Medical Affairs experience in the pharmaceutical industry and/or relevant clinical or scientific experience, including leading scientific publications • Experience developing and executing integrated publication strategies across pre-launch, launch, and post-launch phases • Pipeline portfolio and rare disease experience required • Expert knowledge of good publication practices and guidance, including GPP and ICMJE • Understanding of clinical trial design and execution, statistical methods, and clinical trial data reporting requirements • Ability to define and track publication performance metrics and assess scientific communication impact • Demonstrated leadership skills within large matrixed, cross-functional teams • Experience managing and developing high-performing teams • Strong project management skills, including publication planning, medical and technical writing, editing, and review • Ability to strategically analyze complex data and synthesize scientific information • Excellent written and verbal communication skills • Proficiency with Microsoft Office and document management systems such as PubStrat, SharePoint, Veeva Vault, and Smartsheet • Ability to travel domestically and internationally approximately 25% of the time

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