About this role
About the Role A CRA I at ICON supports clinical trial monitoring activities for oncology programs, delivering high-quality monitoring work onsite in the UK and collaborating with teams and investigators to ensure patient safety and regulatory compliance. What You'll Do
- Deliver clinical trial monitoring to a high standard and coordinate activities for setting up and monitoring a study, including maintaining study documentation and reporting
- Run sponsor-generated queries efficiently and support cost-efficient study management; participate in preparation/review of study documents and feasibility for new proposals
- Develop and maintain strong relationships with stakeholders, investigators, and site staff
- Ensure patient safety through adherence to ICON procedures, protocols, and regulatory requirements What We're Looking For
- University degree in medicine, science, or equivalent
- Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data
- Excellent written and verbal English communication
- Strong interpersonal skills and ability to address queries promptly
- Willingness to travel approximately 60% to sites in the UK and beyond
- Oncology onsite monitoring experience (required) Nice to Have
- Experience in oncology trials and onsite monitoring (if not already listed as required) Compensation & Benefits
- Competitive salary
- Various annual leave entitlements
- Health insurance offerings
- Retirement planning offerings
- Global Employee Assistance Programme LifeWorks (24/7 access to a global network)
- Life assurance and flexible country-specific benefits (childcare vouchers, bike purchase, gym memberships, travel passes, health assessments, etc.)
- ICON inclusion & belonging culture and equal opportunity employer