Senior Director, Late Oncology

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🔥 1 minute ago

🌐 United States, United Kingdom – Remote

🇺🇸 United States – Remote 🇬🇧 United Kingdom – Remote

💵 $230.4k - $345.6k / year

⏰ Full Time

🟠 Senior

👔 Director

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Jazz Pharmaceuticals

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 2003

🏥 Healthcare

🏭 Manufacturing

🧬 Biotechnology

Healthcare • Manufacturing • Biotechnology

Jazz Pharmaceuticals is a biopharmaceutical company dedicated to developing innovative medicines that address serious unmet medical needs. With a strong commitment to research and development, Jazz focuses on creating life-changing therapies, emphasizing the importance of collaboration, diversity, and employee engagement in its operations. The company prides itself on transforming patients' lives through its meaningful product offerings and a culture that fosters enthusiasm and flexibility.

📋 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 governance, resource planning, and operational excellence • Lead end-to-end execution of complex late-phase oncology clinical trials on schedule, within scope, and on budget • Drive operational excellence, risk management, and proactive mitigation across late oncology trials • Establish options analysis and data-driven decision-making frameworks for trial execution challenges • Partner with Clinical Operations, GCDO, Clinical Development, Medical Affairs, Regulatory Affairs, Biometrics, Safety, and R&D leadership • Build relationships with CROs, academic research networks, trial steering committees, and KOLs • Contribute to operational feasibility assessments and early 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 • Directly manage, mentor, and develop Clinical Operations Directors and Associate Directors • Build functional capabilities and ensure Program Leads have the competencies, tools, and resources required • Recruit, retain, and scale clinical operations talent • Promote global team alignment and flexible resourcing across international time zones and geographic regions • Ensure oncology trials adhere to ICH GCP, regulatory standards, and internal SOPs • Drive audit and inspection readiness and contribute to audits, inspections, and regulatory queries • Integrate decentralized clinical trials, patient-centric execution models, and pragmatic trial designs • Adopt digital solutions, automated workflows, and predictive AI analytics • Optimize operational workflows, modernize SOPs, and promote agile ways of working

🎯 Requirements

• Proven, repeatable track record delivering complex clinical trials and multi-country clinical trial portfolios, specifically late-stage Phase 2/3/4 oncology development • Experience partnering directly 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 a global study management or clinical operations organization in pharmaceutical, biotech, or CRO industry • Track record of strategic function leadership, organizational design, and departmental vision setting • Ability to manage complex technical details while maintaining a strategic enterprise perspective • Collaboration with Clinical Development and medical experts to translate scientific concepts into operationally viable study designs and execution plans • Financial and governance acumen, including constructing, analyzing, and presenting integrated program/study budgets and timelines • Capability to operate 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 • Compliance with ICH GCP guidelines, global regulatory standards, and internal SOPs

🏖️ Benefits

• 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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