Clinical Research Associate
ICON · Sao Paulo, Brazil
Clinical OperationsFull-timeCompany career page
RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.
Role summary
Clinical Research Associate position in a sponsor-dedicated model at a leading full-service provider. The role involves managing clinical trial monitoring activities, ensuring protocol compliance and data quality, and collaborating with site investigators across multiple studies.
What they're looking for
- Bachelor's degree in scientific or healthcare-related field
- Minimum 2 years of clinical research associate experience
- Proficiency with ICH-GCP guidelines and clinical trial regulations
- Strong organizational and communication abilities with attention to detail
- Ability to work independently and collaboratively under pressure
- Willingness to travel approximately 60% of the time
What you'll be doing
- Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials
- Ensure protocol compliance, data integrity, and patient safety throughout trial conduct
- Review clinical data and manage query resolution to maintain data quality
- Collaborate with investigators and site staff to support smooth study operations
- Prepare and review study documentation including protocols and clinical study reports
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.