SVP, Pharmaceutical Sciences

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🌲 North Carolina – Distant

🌲 North Carolina – Remote

⏰ Temps Plein

🔴 Expert

👔 Vice-président

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BioCryst Pharmaceuticals, Inc.

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501 - 1000 employés

🧬 Biotechnologie

💊 Pharmaceutique

💰 €450 000 000 Post-IPO Debt - BioCryst Pharmaceuticals en 2023-04

Biotechnology • Pharmaceuticals

BioCryst Pharmaceuticals, Inc. est une entreprise mondiale de biotechnologie spécialisée dans la découverte, le développement et la commercialisation de nouvelles petites molécules orales et de thérapies protéiques pour les maladies rares, notamment l'œdème angioneurotique héréditaire (OAH). Fondée en 1986, BioCryst utilise la conception de médicaments guidée par la structure, la chimie médicinale et les technologies avancées pour développer des médicaments de première classe ou de meilleure classe, et travaille en étroite collaboration avec les patients, les associations de patients et les partenaires mondiaux pour mettre les traitements sur le marché.

Description

• Align project priorities, coordinate PharmSci activities, project deliverables and resources between PharmSci and other Developmental functions in BioCryst. • Mentor and develop a high performing PharmSci leadership team that efficiently coordinates activities across different PharmSci functional areas. • Maintain seamless collaboration with other functional areas of the organization to ensure project progress according to agreed timelines especially research and discovery. • Work closely with Clinical, Quality, Regulatory, Technical Operations, Preclinical and Finance functions in the company in the development and execution of PharmSci plans to meet corporate objectives. • Serve as a member of the Technical Operations leadership team, contributing to enterprise operational strategy, governance, and execution. • Create, maintain, and curate the PharmSci technology roadmap across biologics and small molecules to guide platform capabilities, externalization strategy, and investment priorities. • Oversee and facilitate PharmSci technology transfers and process validation readiness in collaboration with Technical Operations to support manufacturing for drug substance and drug product at contract manufacturing organizations. • Review and approve PharmSci and GMP related submission documents to assure compliance with regulatory standards and ensure their suitability for regulatory submissions. • Drive a culture of scientific rigor, operational excellence, and continuous improvement across PharmSci functional teams and external partners. • Participate and advise in the HR initiated leadership development programs for PharmSci personnel.

🎯 Exigences

• PhD in science or engineering or an equivalent combination of education and experience. • Minimum of 15+ years’ experience in all phases of drug development of oral and sterile products, preferably gained in an industrial setting. • Demonstrated breadth of experience across modalities, including biologics and small molecules, with end-to-end PharmSci leadership from early development through commercial readiness. • Track record of partnering effectively across Research, Clinical, Regulatory, Quality, and Technical Operations in a matrix environment to deliver robust, compliant PharmSci packages and supply strategies for global development programs. • Experience with the preparation of multiple US and global applications (IND, IMPD, NDA, and BLA). • Exceptional oral and written communication and presentation skills.

🏖️ Avantages

• Health insurance • Flexible work arrangements • Professional development