Senior Clinical Trial Manager (CNS)

CNS & Rare Disease 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 ; Alzheimer's disease, Dementia, Multiple Sclerosis or other Rare Disease 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

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