Clinical Trial Manager - ICO (Peri-Approval & Observational Research)
About the role
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- Primary point of contact for Clinical Operations aspects of designated projects and responsible for developing successful working relationships with clients
- Responsible for planning, scheduling and implementing the Clinical Operations aspects of projects
- Contribute to the development and maintenance of cross functional project management plans
- Responsible for risk mitigation strategies, associated action plan and issue resolution
- Responsible for managing the Clinical Operations project team, including ensuring all necessary project training is provided to assigned staff
- Provide direction and support to the Clinical Operations study team
- Collaborate with Business Development (BD) to ensure timely completion of change orders
- Track Clinical Operations project deliverables using appropriate tools
- A satisfactory progression of monitoring experience, along with previous experience in leadership and/or management activities
- Previous working experience within the clinical trial management field.
- Experience in Late Phase monitoring a plus.
- Business level in written and spoken English.
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. See all locations Learn more about Our Culture at ICON
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