Sr CRA I
Fortrea · Buenos Aires, Argentina
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
Senior Clinical Research Associate responsible for site monitoring, site management, and regulatory compliance across clinical studies. Leads projects of limited scope and manages study sites according to sponsor procedures and regulatory guidelines.
What they're looking for
- University degree in life science or clinical research certification; or 3+ years pharmaceutical/CRO clinical research experience
- 3+ years clinical monitoring experience with advanced site monitoring and management skills
- Thorough knowledge of regulatory requirements and drug development process
- Fluent in local office language and English, both written and verbal
- Strong SAE reporting understanding and independent CRF review capability
- Valid driver's license and ability to work with minimal supervision
- Proficiency with computer systems and data management platforms
What you'll be doing
- Conduct site monitoring, pre-study visits, and study closeout; maintain accurate study files and documentation
- Verify informed consent adherence, protocol compliance, and data integrity through source document review
- Manage site resources efficiently and ensure audit readiness at site level
- Prepare trip reports, coordinate with vendors, and negotiate study budgets with investigators
- Track and report Serious Adverse Events; perform CRF reviews and query management independently
Privacy & handoff
This role links to Fortrea'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.