Global Study Manager
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Job Description
Global Study Manager overseeing clinical trials for ICON’s sponsor-dedicated research programmes. Coordinating protocols, stakeholders, compliance, vendors, and study delivery across Europe.
Responsibilities:
- Manage day-to-day clinical trial management activities
- 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 relationships with trial investigators and stakeholders
- Ensure trials comply with local, national, and international regulations and ethical guidelines
- Problem-solve and make critical decisions regarding trial design, vendor selection, and risk management
- Support the team and stakeholders to deliver high-quality outcomes across clinical programmes
Requirements:
- University degree in medicine, science, or equivalent combination of education & experience
- Solid clinical trial management 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%)
- Legal right to work in the country where the role is based
Benefits:
- 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
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