About this role
About the Role ICON plc is a world-leading healthcare intelligence and clinical research organization. As a CRA at ICON, you will contribute to our clinical trial operations function, working collaboratively to deliver high-quality outcomes across our clinical programmes. What You'll Do
- Deliver clinical trial monitoring work to a high standard, working closely with your team and stakeholders
- Coordinate all activities for setting up and monitoring a study, complete accurate study status reports and maintain study documentation
- Run sponsor-generated queries efficiently and take responsibility for study cost efficiency; participate in the preparation and review of study documentation and feasibility studies for new proposals as required
- Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff
- Ensure patient safety by ensuring compliance with ICON's procedures, protocols, and regulatory requirements What We're Looking For
- University degree in medicine, science, or equivalent
- Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data
- Excellent written and verbal communication in English
- Prior monitoring experience, minimum 12 months after being certified as per Italian law
- Good social skills enabling you to deal with queries in a timely manner
- Willingness to travel as required (approximately 60%) Nice to Have Compensation & Benefits Our benefits include: competitive salary; annual leave entitlements; health insurance; retirement planning; LifeWorks Global Employee Assistance Programme; Life assurance; flexible country-specific optional benefits (including childcare vouchers, bike purchase schemes, discounted gym memberships, travel passes, health assessments); and more. ICON offers an inclusive culture with equal opportunity and focus on well-being and work-life balance. Visit our careers site to read more about the benefits ICON offers.