Global Study Associate Director
ICON · Blue Bell +2 more
Clinical OperationsFull-timeCompany career page
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Role summary
ICON Strategic Solutions seeks a Global Study Associate Director for oncology clinical trials. The role involves leading cross-functional study teams, managing external service providers, overseeing study documentation and budgets, and ensuring regulatory compliance across multiple global sites.
What they're looking for
- University degree in medical, biological sciences, or clinical research discipline
- 5+ years clinical experience in pharmaceutical industry trial management
- Demonstrated experience overseeing large global clinical trial projects
- Required experience managing oncology studies or projects
- Legal right to work in country where role is based
What you'll be doing
- Lead cross-functional study teams and oversee outsourced activities to meet timelines, budgets, and quality standards
- Manage communication across functions, external partners, and conduct investigator meetings
- Develop and maintain study plans including quality and risk management strategies
- Oversee Trial Master File completion and ensure ongoing regulatory compliance and inspection readiness
- Manage study budgets, re-forecast expenses, and provide progress reports to clinical project teams
Privacy & handoff
This role links to ICON's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.