SVP, Pharmaceutical Sciences

🕒 April 8

🌲 North Carolina – Remote

🌲 North Carolina – Remote

⏰ Full Time

🔴 Lead

👔 Vice President

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BioCryst Pharmaceuticals, Inc.

WebsiteLinkedInAll Job Openings

501 - 1000 employees

🧬 Biotechnology

💊 Pharmaceuticals

💰 $450M Post-IPO Debt - BioCryst Pharmaceuticals on 2023-04

Biotechnology • Pharmaceuticals

BioCryst Pharmaceuticals, Inc. is a global biotechnology company focused on the discovery, development, and commercialization of novel oral small-molecule and protein therapeutics for rare diseases, notably hereditary angioedema (HAE). Founded in 1986, BioCryst uses structure-guided drug design, medicinal chemistry, and advanced technologies to develop first-in-class or best-in-class medicines, and works closely with patients, advocacy groups, and global partners to bring treatments to market.

📋 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.

🎯 Requirements

• 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.

🏖️ Benefits

• Health insurance • Flexible work arrangements • Professional development