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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.
Job Responsibility
Manage clinical trial operations activities
Plan, execute and report from country feasibility up to and including site initiation for assigned innovative medicines phase I-IV studies
Act as single point of contact and local study team lead within the country/cluster
Support study feasibility and country patient commitments
Lead site selection
Ensure study start-up activities are conducted and completed on time
Oversee local vendor selection and performance
Drive the conduct of the study and track status
Ensure recruitment targets are met
Oversee local clinical team activities
Lead/chair local study team meetings
Coordinate study handover process
Conduct or coordinate training for CRAs
Conduct or coordinate local investigator meetings
Monitor site budget and contract negotiations
Track study budget
Requirements
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%)
What we offer
Various annual leave entitlements
A range of health insurance offerings
Competitive retirement planning offerings
Global Employee Assistance Programme
Life assurance
Flexible country-specific optional benefits including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments