About this role
Job title: Clinical Research Associate I
About the Role
ICON plc is seeking a Clinical Research Associate I for a sponsor-dedicated academy to contribute to clinical trial operations across our programmes. You will work with a team to deliver high-quality monitoring outcomes while ensuring patient safety and regulatory compliance.
What You'll Do
- Deliver clinical trial monitoring to a high standard and collaborate with the 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 participate in cost-efficiency efforts; assist in 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 complying with ICON 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 social skills enabling you to handle queries in a timely manner.
- Willingness to travel approximately 60%.
Compensation & Benefits
- Competitive salary.
- 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 professionals.
- Life assurance.
- Flexible country-specific optional benefits (e.g., childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments).