Senior Director, Global Study Management

🔥 10 hours ago

🌐 United States, United Kingdom – Remote

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

💵 $236k - $354k / year

⏰ Full Time

🟠 Senior

👔 Director

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

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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 and articulate the strategic vision and long-term direction for Global Study Management • Contribute to Clinical Operations governance, resource planning, and operational excellence • Foster a high-performance, inclusive culture across Global Study Management • Partner with Program Leadership and Strategic Trial Optimization on clinical trial portfolio planning and execution • Oversee trial execution against KPIs, timelines, quality standards, and budget targets • Provide direction and resolve escalated operational challenges • Lead, mentor, and develop Global Study Management leaders • Build and scale functional capabilities, tools, and resources for complex trials • Promote global team alignment and flexible resourcing across international time zones and regions • Partner with Clinical Development Operations, Clinical Development, Regulatory Affairs, Biostatistics, Quality Assurance, and Global Supply Chain • Drive financial stewardship, trial forecasting, resource allocation, and cost optimization • Ensure adherence to ICH GCP, global regulatory requirements, and company SOPs • Drive audit and inspection readiness across trial management activities

🎯 Requirements

• Demonstrated track record leading complex, global Phase I–IV clinical study execution across multiple therapeutic areas • Extensive leadership experience within a global study management or clinical operations organization in the biopharmaceutical industry or CRO • Demonstrated strategic functional leadership, organizational design, and departmental vision-setting experience • 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 • Ability to construct, analyze, and optimize functional workforce budgets • Ability to operate effectively across a matrixed global environment with time zone flexibility • Superior communication, negotiation, and stakeholder management skills • Bachelor's degree in Life Sciences, Allied Health, or related field required • Direct line management required • Experience in oncology, rare disease, or neuroscience preferred • Advanced degree (MS, PharmD, PhD, or MBA) strongly preferred • Leadership of people managers preferred

🏖️ Benefits

• Discretionary annual cash bonus or incentive compensation • Discretionary equity grants under the Long Term Equity Incentive Plan • Medical insurance • Dental insurance • Vision insurance • 401k retirement savings plan • Flexible paid vacation

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