About this role
About the Role ICON is seeking a Junior Clinical Research Associate (CRA I) dedicated to sponsor-dedicated clinical trial monitoring. The role involves delivering high-quality monitoring work, coordinating setup and monitoring activities, and ensuring patient safety and regulatory compliance across our clinical programmes. What You'll Do
- Deliver clinical trial monitoring work to a high standard, collaborating 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; participate in preparation and review of study documentation and feasibility studies for new proposals as required; contribute to study cost efficiency.
- 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
- 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 approximately 60%. Compensation & Benefits
- Various annual leave entitlements.
- Health insurance options to suit you and your family.
- Competitive retirement planning offerings.
- Global Employee Assistance Programme (LifeWorks) with 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).