Clinical Trial Manager (Oncology)
About the role
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Oncology and Hematology Specialism
The role
- Contribute to the development and maintenance of cross functional project management plans; supply risk mitigation strategies, associated action plan and issue resolution
- Responsible for owning the Clinical Operations project team, including ensuring all necessary project training built in for assigned staff
- Provide direction and support to the Clinical study team
- Collaborate with Business Development (BD) to act on timely completion of change orders
- Track Clinical project deliverables, using appropriate tools to action
What you need
- ICON is seeking experience in relevant therapeutic areas outlined above ; Oncology, solid tumors or Hematology indications
- University/Bachelor’s Degree in medicine, science or equivalent degree/experience
- Thorough understanding of ICH GCP and relevant regulations for the conduct of clinical trials
- Fluent in written and spoken English
- Due to the nature of this position, the employee will travel approx. 25%. Therefore, dependent on the employee’s location, the employee may be required to possess a valid Driver’s license
- This position is open to be based in any of ICON European locations and includes flexibility to work full or part-time home based, depending on your proximity to an ICON office
Benefits of Working in ICON

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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