9 дней назад
Executive Director, Global Site & Study Operations, Americas (Clinical Operations)
263 760 - 356 852$
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
Executive Director, Global Site & Study Operations, Americas (Clinical Operations): Leading regional clinical trial site and study operations across the Americas with an accent on portfolio strategy, compliance, resource allocation, and geographically distributed leadership. Focus on overseeing Phase I–IV trial delivery, strengthening monitoring and site engagement models, managing operational risks, and driving digital and organizational transformation.
Location: Thousand Oaks, California, United States
Salary: $263,760–$356,852 annual base salary
Company
is a biotechnology company developing medicines across oncology, inflammation, general medicine, rare disease, and obesity-related conditions.
What you will do
- Lead regional Study & Site Operations across the Americas, including the United States, Canada, and Latin America.
- Oversee the initiation, management, quality, execution, and closeout of Phase I–IV clinical trials.
- Set regional strategies for site engagement, monitoring, resource allocation, vendor performance, and budget utilization.
- Provide executive oversight of high-risk and strategically important clinical programs, including risk mitigation and escalation.
- Represent the region in global governance forums and influence portfolio, timeline, and resourcing decisions.
- Drive continuous improvement through digital solutions, predictive analytics, modern monitoring approaches, and operating-model transformation.
Requirements
- Doctorate degree and 6 years of global site study experience, or master’s degree and 10 years, or bachelor’s degree and 12 years.
- At least 6 years of managerial or team leadership experience.
- Bachelor’s degree in life sciences, pharmacy, nursing, medicine, or a related discipline; an advanced degree is preferred.
- 15+ years of progressive experience in pharmaceutical, biotechnology, CRO, or clinical research organizations.
- Extensive experience leading clinical operations, study management, geographically distributed teams, and clinical trial portfolios across multiple development phases.
- Strong knowledge of ICH-GCP, regulatory requirements, clinical quality management, CRO/vendor governance, budgets, and resource planning.
Nice to have
- Experience supporting regulatory inspections and working with clinical research vendors, central laboratories, or imaging vendors.
- Experience managing clinical operations across the Americas and understanding local clinical-trial regulations.
Culture & Benefits
- Collaborative, inclusive, science-based environment focused on serving patients.
- Health, dental, vision, life, disability, and flexible spending benefits.
- Retirement and savings plan with company contributions.
- Annual bonus program and stock-based long-term incentives.
- Paid time off, company-wide shutdowns, and career development opportunities.
- Flexible work models may be available where applicable; sponsorship is not guaranteed.
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