About this role
About the Role ICON plc is seeking a Clinical Research Associate to oversee and coordinate clinical trials, ensuring regulatory compliance and accurate data collection across studies. This role supports ICON's mission to drive innovation in clinical development and requires collaboration with investigators, sites, and sponsors. What You'll Do
- Work independently to 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.
- Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff.
- Ensure patient safety by complying with ICON's procedures, protocols, and regulatory requirements. What We're Looking For
- At least 2 years of monitoring experience as a CRA.
- University degree in medicine, science, or equivalent.
- Knowledge of ICH-GCP guidelines and ability to review/evaluate medical data.
- Excellent written and verbal communication in English.
- Strong interpersonal skills enabling timely handling of queries.
- Ability to travel at least 60% of the time (international and domestic) and a valid driver's license. Compensation & Benefits
- Competitive salary and benefits tailored to the country; includes annual leave entitlements and health insurance options.
- Retirement planning offerings and access to LifeWorks Global Employee Assistance Programme (24/7).
- Life assurance and flexible country-specific benefits (childcare vouchers, gym discounts, travel passes, health assessments, and more).
- ICON's commitment to inclusion, belonging, and a discrimination-free workplace.