About this role
About the Role ICON plc is a world-leading healthcare intelligence and clinical research organization. As a CRA I at ICON, you will contribute to our clinical trial operations by delivering high-quality monitoring activities and collaborating with teams to drive study success. What You'll Do
- Deliver clinical trial monitoring work to a high standard, working closely 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 and take responsibility for study cost efficiency; 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. What We're Looking For
- University degree in medicine, science, or equivalent.
- 6 months of experience as Clinical Research Associate on site.
- 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%).
- Based in Buenos Aires, Argentina. Compensation & Benefits
- Competitive salary and a range of additional benefits as outlined by ICON. Benefits examples include: various annual leave entitlements, health insurance offerings, competitive retirement planning, LifeWorks global EAP, life assurance, and flexible, country-specific optional benefits such as childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, and health assessments.
- Visit our careers site to read more about the benefits ICON offers.