Clinical Research Associate
ICON · Sao Paulo, Brazil
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Role summary
A Clinical Research Associate will conduct clinical trial monitoring and coordinate study setup activities at this global healthcare research organization in São Paulo. Responsibilities include managing sponsor queries, maintaining documentation, ensuring regulatory compliance, and building stakeholder relationships. The position requires a degree in medicine or science, ICH-GCP knowledge, strong English communication skills, and willingness to travel approximately 60%.
What they're looking for
- University degree in medicine, science, or equivalent field
- Clinical trial monitoring experience
- Knowledge of ICH-GCP guidelines and medical data evaluation
- Excellent written and verbal English communication skills
- Strong interpersonal skills for managing stakeholder queries
- Willingness to travel approximately 60% of the time
- Legal right to work in the role's country of employment
What you'll be doing
- Coordinate study setup and monitoring activities independently while maintaining accurate documentation
- Process sponsor-generated queries and manage study cost efficiency
- Review study documentation and conduct feasibility assessments for new proposals
- Build and maintain collaborative relationships with investigators and site staff
- Ensure regulatory compliance and patient safety across clinical programmes
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.