About this role
About the Role
ICON plc is a world-leading healthcare intelligence and clinical research organization. In this role you will own end-to-end study start-up activities, ensuring timelines, quality standards, and regulatory requirements are met, while working fully remote in the UK within ICON's growing program. What You'll Do
- Leading the study start-up strategy and execution for assigned trials
- Managing site activation timelines, milestones, and deliverables
- Partnering with regulatory, clinical, and external stakeholders to ensure smooth start-up processes
- Overseeing site selection, feasibility, and activation activities
- Identifying risks and proactively implementing solutions to keep studies on track
- Ensuring compliance with all local and global regulatory requirements What We're Looking For
- Solid experience in clinical operations and study start-up within a CRO or pharma environment
- Full right to work in the UK
- Strong project management skills with the ability to manage multiple priorities
- Excellent stakeholder management and communication skills
- A proactive, solution-focused mindset with high attention to detail
- Ability to thrive in a fast-paced, global environment Compensation & Benefits
- Competitive salary
- Various annual leave entitlements
- Health insurance offerings
- Competitive retirement planning offerings
- Global Employee Assistance Programme LifeWorks with 24-hour access to a global network of professionals
- Life assurance
- Flexible country-specific optional benefits (e.g., childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others)