ICON

Global Study Manager

In short

This role manages day-to-day clinical trial operations for a sponsor-dedicated program at ICON, a large FSP organisation with over 90 sponsor partnerships. It covers planning trials, ensuring compliance with regulations and ethical guidelines, managing relationships with investigators and stakeholders, and making decisions on trial design, vendors, and risk. It requires a university degree in medicine or science, demonstrated clinical trial management experience, therapeutic-area expertise, and willingness to travel about 25% of the time; monitoring experience is preferred.

Global Study Manager
At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise.
As the world's largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.
As a Clinical Trial Manager at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programmes.
What You Will Do
You will manage day-to-day clinical trial management activities, supporting your team to deliver quality outcomes.
Key responsibilities include:
•Plan and manage all aspects of clinical trials, ensuring adherence to timelines, budget, and quality standards.
•Collaborate with cross-functional teams to establish and implement clinical trial protocols and procedures.
•Build and manage strong relationships with trial investigators and stakeholders.
•Ensure all trials are conducted in compliance with local, national, and international regulations and ethical guidelines.
•Problem-solve and make critical decisions regarding trial design, vendor selection, and risk management.
Your Profile
You will have solid clinical trial management experience, with the ability to manage competing priorities and develop your team.
Required qualifications and experience:
•University degree in medicine, science, or equivalent combination of education & experience
•Demonstrated ability to drive the clinical deliverables of a study
•Subject matter expertise in the designated therapeutic area
•Prior monitoring experience is preferred
•Willingness to travel as required (approximately 25%)
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
•Competitive base salary and performance related incentives
•Health and wellbeing programmes including medical, dental, and vision coverage where applicable
•Retirement and pension plans
•Life assurance and disability coverage
•Employee assistance programmes and wellbeing resources
•Learning and development opportunities through structured training and career pathways
Benefits may vary depending on role and location.

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