Clinical Trial Director
hace 4 días
At ICON, you will be joining a world-class clinical research organization dedicated to saving lives and improving human health. Our mission is to accelerate the development of medicines that make a difference in people's lives.
The role of a Clinical Trial Manager at ICON is crucial in ensuring the successful execution of clinical studies. As a Clinical Trial Manager, you will be responsible for planning, managing, and overseeing the execution of clinical studies in accordance with the global program strategy. This involves leading a cross-functional Local Study Team (LST) to ensure timely delivery, quality, and compliance with regulatory requirements.
Key Responsibilities:
- Plan, manage, and oversee the execution of clinical studies
- Lead the Local Study Team (LST) to ensure timely delivery, quality, and compliance with regulatory requirements
- Contribute to the development of program/study-specific materials, such as monitoring plans and training documents
- Accountable for site-level goal setting and study-specific deliverables for clinical sites within their country/ies
- Provide oversight and monitoring of applicable vendor activities, such as laboratory and equipment provisioning
- Collaborate with local teams to ensure country-level study delivery aligns with global expectations
- Identify and facilitate resolution of cross-functional study-specific issues
- Evaluate and implement risk mitigation strategies, informing the CST/TMT, LST, and local teams of risks associated with delivery
Requirements:
- Bachelor's degree in a health, life sciences, or other relevant field of study
- Minimum 5-6 years' work experience in clinical research or project management and site management
- CRA experience preferred
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