CRA I

About the Role ICON is seeking a CRA I to contribute to our clinical trial operations function, delivering high-quality monitoring across clinical programmes. You will work closely with your team and stakeholders to ensure patient safety and regulatory compliance while helping drive delivery of trials. What You'll Do

• Deliver clinical trial monitoring to a high standard and coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation.
• Run sponsor-generated queries efficiently and 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.
• Travel approximately 60% as required. 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.
• Good social skills enabling you to deal with queries in a timely manner.
• Willingness to travel as required (approximately 60%). Compensation & Benefits
• Competitive salary.
• Various annual leave entitlements.
• A range of health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings to maximize savings.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of professionals who support well-being.
• Life assurance.
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers.