Study Start-Up CRA
ICON · Buenos Aires, Argentina
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
ICON seeks an experienced Clinical Research Associate to lead study start-up activities and oversee clinical trial monitoring in Buenos Aires. The role involves ensuring protocol adherence, conducting site visits, and guiding site staff while maintaining regulatory compliance and data integrity standards.
What they're looking for
- Bachelor's degree in scientific or healthcare-related discipline
- Extensive CRA experience with clinical trial processes and regulatory knowledge
- Proficiency in monitoring practices, data integrity, and clinical trial software
- Advanced English language proficiency
- Willingness to travel approximately 20% as required
- Legal authorization to work in Argentina
What you'll be doing
- Monitor clinical trial sites for protocol adherence and GCP standard compliance
- Conduct site visits to assess performance, resolve issues, and provide operational support
- Collaborate with cross-functional teams on timely data collection and reporting
- Train site staff and other CRAs on clinical trial conduct standards
- Build and maintain effective relationships with site personnel and stakeholders
Privacy & handoff
This role links to ICON's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.