Senior CRA
ICON · Sao Paulo, Brazil
Clinical OperationsFull-timeCompany career page
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Role summary
Senior Clinical Research Associate needed to oversee clinical trial activities at multiple sites in São Paulo, Brazil. Responsible for monitoring protocol adherence, regulatory compliance, and quality assurance while leading a team of site staff and junior CRAs.
What they're looking for
- Bachelor's degree in scientific or healthcare-related field
- Extensive Clinical Research Associate experience with deep knowledge of trial processes
- Proven ability to manage multiple sites and projects concurrently
- Expert-level monitoring practices, data integrity, and site management skills
- Strong communication and stakeholder management abilities
- Willingness to travel approximately 60% of the time
What you'll be doing
- Monitor clinical trial sites for protocol adherence, regulatory compliance, and GCP standards
- Conduct site visits to assess performance, resolve issues, and provide operational support
- Collaborate with cross-functional teams on timely and accurate data collection and reporting
- Train and mentor site staff and junior CRAs on clinical trial conduct standards
- Build and maintain relationships with site personnel and stakeholders to ensure trial success
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.