VP, Global Clinical Development

🔥 13 hours ago

🌲 North Carolina – Remote

🌲 North Carolina – Remote

⏰ Full Time

🔴 Lead

👔 Vice President

👻 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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BioCryst Pharmaceuticals, Inc.

WebsiteLinkedInAll Job Openings

501 - 1000 employees

🏥 Healthcare

💼 Consulting

📦 Logistics

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

Healthcare • Consulting • Logistics

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

• Provide strategic leadership for personnel management, operations, matrix team integration, and clinical development planning • Ensure efficient and productive clinical development across all stages of drug development • Lead development and implementation of initiatives coordinating the company’s clinical programs • Integrate the strategic clinical plan into research and product development missions • Oversee performance against trial metrics, organizational objectives, and operational strategy • Lead changes in Clinical Development functions to scale and deliver high-quality clinical trials across assets and indications • Set goals and evaluate performance for direct reports and the department • Support career paths, training, and leadership development plans • Manage departmental budgets and resourcing strategy • Build quality-focused clinical infrastructure and implement corrective actions • Develop SOPs aligned with regulatory requirements and ensure consistent implementation and documentation • Ensure inspection readiness of active and completed studies • Set outsourcing strategy and oversee vendors, CROs, and escalation management • Collaborate with stakeholders on trial design, scientific rigor, regulatory pathways, and pipeline advancement • Participate in governance bodies and processes including Portfolio Review Committee, stage gate reviews, and Development Review Group • Develop communications presenting company programs and products to prospective KOLs and investigators • Champion patient-focused clinical development and represent patient advocacy and voice in trial planning, design, and conduct

🎯 Requirements

• MD with a minimum of 10 years pharmaceutical development experience, preferably gained in a sponsor and/or CRO role • At least 5 years in a senior management role or an equivalent combination of education and experience • Demonstrated drug development experience within the biotech/pharmaceutical industry • Expertise in clinical trial design, conduct, analysis, and interpretation of scientific data • Experience building, training, mentoring, and motivating clinical development teams in industry • Highly developed line management and matrix team skills, including collaboration and influencing across functions at senior level • Ability to multitask across a broad range of activities and maintain strong priorities • Driven to progress programs and timelines at very rapid speeds • Equal employment opportunity compliance and applicable work authorization requirements