Senior CRA
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
Senior Clinical Research Associate at ICON overseeing clinical trial monitoring activities across multiple sites in a sponsor-dedicated model. The role emphasizes protocol adherence, regulatory compliance, and quality assurance while providing mentorship and cross-functional collaboration in Brazil.
What they're looking for
- Bachelor's degree in scientific or healthcare-related discipline
- Extensive Clinical Research Associate experience with clinical trial processes and regulatory knowledge
- Ability to manage multiple sites and projects simultaneously with strong organizational skills
- Expertise in monitoring practices, data integrity, and clinical trial software systems
- Excellent communication and stakeholder management capabilities
- Willingness to travel approximately 60% as required
- Legal right to work in Brazil
What you'll be doing
- Monitor clinical trial sites for adherence to study protocols, regulatory requirements, and GCP standards
- Conduct on-site assessments to evaluate performance, resolve operational issues, and provide support
- Collaborate with cross-functional teams to ensure timely and accurate data collection and reporting
- Train site staff and junior CRAs to maintain high standards of clinical trial conduct
- Establish and maintain effective working 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.