About this role
About the Role
ICON is a world-leading healthcare intelligence and clinical research organization. As a CRA I 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, coordinating 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 study cost efficiency; assist 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.
- Good interpersonal and communication skills enabling you to deal with queries in a timely manner.
- Willingness to travel as required (approximately 60%). Compensation & Benefits
- Competitive salary with additional benefits.
- Various annual leave entitlements.
- Health insurance offerings to suit you and your family’s needs.
- Competitive retirement planning offerings.
- Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
- Life assurance and flexible country-specific optional benefits (e.g., childcare vouchers, bike purchase schemes, gym memberships, subsidized travel passes, health assessments).