Senior Director, Early Oncology

🕒 il y a 1 jour

🌐 États-Unis, Royaume-Uni – Distant

🇺🇸 États-Unis – Télétravail 🇬🇧 Royaume-Uni – Télétravail

💵 $230 400 - $345 600 / an

⏰ Temps Plein

🟠 Senior

👔 Directeur

🦅 Parrain de Visa H1B

Cette entreprise a parrainé des visas H1B par le passé.

👻 Score fantôme 0%

Ce que ça veut dire : la probabilité que personne ne recrute vraiment pour cette offre.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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Jazz Pharmaceuticals

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1001 - 5000 employés

Fondée en 2003

🏥 Santé

🏭 Fabrication

🧬 Biotechnologie

Healthcare • Manufacturing • Biotechnology

Jazz Pharmaceuticals est une entreprise biopharmaceutique dédiée au développement de médicaments innovants répondant à des besoins médicaux sérieux non satisfaits. Avec un fort engagement envers la recherche et le développement, Jazz se concentre sur la création de thérapies transformatrices, mettant en avant l'importance de la collaboration, de la diversité et de l'engagement des employés dans ses opérations. L'entreprise est fière de transformer la vie des patients grâce à ses offres de produits significatives et une culture qui favorise l'enthousiasme et la flexibilité.

Description

• Define the strategic vision and long-term direction for Late Oncology Program Management / Early Phase Program Management • Serve on the Clinical Operations Leadership Team and contribute to department governance, resource planning, and operational excellence • Foster a high-performance, inclusive culture across the organization • Ensure end-to-end execution of complex global early-phase Phase 1 and 1b oncology clinical trials on schedule, within scope, and on budget • Drive operational excellence, risk management, and proactive mitigation across early-phase trials • Establish options analysis and data-driven decision-making frameworks • Partner with Clinical Operations, GCDO, Clinical Development, Medical Affairs, Regulatory Affairs, Biometrics, Safety, R&D leadership, CROs, academic research networks, steering committees, and KOLs • Contribute to operational feasibility assessments and execution planning during study concept and protocol development • Develop, review, and defend global clinical program budgets and integrated timelines for governance committees and R&D leadership • Oversee financial planning, trial forecasting, resource allocation, and cost optimization • Define vendor strategy, performance metrics, and governance structures with Strategic Outsourcing and Clinical Innovation • Participate in executive vendor reviews, steering committees, and contract issue escalations • Directly manage, mentor, and develop Clinical Operations Directors and Associate Directors • Build functional capabilities and provide Program Leads with competencies, tools, and resources • Recruit, retain, and scale clinical operations talent • Promote global alignment and flexible resourcing across time zones and regions • Ensure oncology trials comply with ICH GCP, global regulatory standards, and Jazz SOPs • Drive audit and inspection readiness and support audits, inspections, and regulatory queries • Integrate decentralized clinical trials, patient-centric execution models, and pragmatic trial designs • Lead adoption of digital solutions, automated workflows, and predictive AI analytics • Optimize workflows, modernize SOPs, and promote agile ways of working

🎯 Exigences

• Demonstrated track record delivering complex clinical trials and multi-country portfolios, specifically early-phase (Phase 1) oncology • Experience partnering with Clinical Development Leads on program strategy, study design, protocol feasibility, and execution planning • Experience developing, presenting, and overseeing multi-million-dollar clinical trial budgets and complex timelines • Substantial leadership experience within global study management or clinical operations in the pharmaceutical, biotech, or CRO industry • Demonstrated strategic function leadership, organizational design, and departmental vision setting • Ability to manage complex technical details while maintaining a strategic enterprise perspective • Experience collaborating with Clinical Development and medical experts to translate scientific concepts into operationally viable study designs and execution plans • Expertise constructing, analyzing, and presenting integrated program/study budgets and timelines • Ability to operate effectively across a matrixed global environment with time zone flexibility • Superior communication, negotiation, and stakeholder management skills • Advanced degree (Ph.D., Pharm.D., M.S., or equivalent) in a life sciences, clinical research, or healthcare-related discipline preferred • Bachelor’s degree with exceptional industry experience will also be considered • Significant biopharmaceutical industry experience in clinical trial operations, with significant senior leadership responsibility in global study management • Direct line management required, including leadership of people managers preferred • For US-based candidates, must satisfy applicable US work eligibility requirements implied by the US-based compensation section

🏖️ Avantages

• Discretionary annual cash bonus or incentive compensation • Discretionary equity grants • Medical insurance • Dental insurance • Vision insurance • 401k retirement savings plan • Flexible paid vacation

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