Senior Director, Early Oncology

🕒 vor 5 Tagen

🌐 Vereinigte Staaten, Vereinigtes Königreich – Remote

🇺🇸 Vereinigte Staaten – Remote 🇬🇧 Vereinigtes Königreich – Remote

💵 $230.400 - $345.600 / Jahr

⏰ Vollzeit

🟠 Senior

👔 Direktor

🦅 H1B-Visum-Sponsor

Dieses Unternehmen hat in der Vergangenheit H1B-Visa gesponsert.

👻 Geisterscore 0%

Was es bedeutet: die Wahrscheinlichkeit, dass für diese Stelle niemand wirklich einstellt.So liest du es: 60 % oder höher heißt, wir halten das für einen Geisterjob. Niedrigere Werte sind weniger bedenklich.Wie wir werten: Dauer offen, Neuveröffentlichungen, offene Stellen vs Teamgröße, wie schnell Stellen geschlossen werden, und ob ein Gehalt angegeben ist.Hinweis: eine Schätzung aus öffentlichen Daten, kein Urteil über das Unternehmen. Echte Stellen können hoch punkten, nutze es also als Hinweis, nicht als Fakt.

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Jazz Pharmaceuticals

WebsiteLinkedInAlle Stellen

1001 - 5000 Mitarbeiter

Gegründet 2003

🏥 Gesundheitswesen

🏭 Fertigung

🧬 Biotechnologie

Healthcare • Manufacturing • Biotechnology

Jazz Pharmaceuticals ist ein biopharmazeutisches Unternehmen, das sich der Entwicklung innovativer Medikamente widmet, um ernsthafte ungedeckte medizinische Bedürfnisse zu adressieren. Mit einem starken Engagement für Forschung und Entwicklung konzentriert sich Jazz auf die Schaffung lebensverändernder Therapien und betont dabei die Bedeutung von Zusammenarbeit, Vielfalt und Mitarbeiterengagement in seinen Prozessen. Das Unternehmen ist stolz darauf, die Leben der Patienten durch seine bedeutungsvollen Produktangebote zu transformieren und eine Kultur zu fördern, die Begeisterung und Flexibilität unterstützt.

Beschreibung

• 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

🎯 Anforderungen

• 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

🏖️ Vorteile

• 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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