When our values align, there's no limit to what we can achieve.
 
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

Clinical Research Associate (CRA) - Sao Paulo or Rio de Janeiro

Be the Driving Force Behind Clinical Trial Success

About This Role

As a Clinical Research Associate at Parexel, you'll be more than a monitor—you'll be a strategic partner and the primary point of contact for clinical sites throughout the entire trial lifecycle. From site identification through close-out, you'll own site performance, build meaningful relationships, and solve complex challenges to ensure trial success while protecting patient safety and data integrity.

This is a dynamic role where you'll combine relationship management, strategic thinking, and regulatory expertise to drive sites to peak performance.

What You'll Do

• Monitor Clinical Trials: Conduct site monitoring visits to ensure protocol compliance, data quality, and patient safety
• Build Relationships: Partner with investigative sites to foster strong, collaborative relationships
• Ensure Quality: Review and verify source documents, case report forms, and essential documentation
• Problem-Solve: Identify and resolve site-level issues proactively
• Guide & Educate: Provide training and guidance to site staff on protocol requirements and GCP standards
• Travel: Visit clinical sites within your assigned territory (aprox 5 visits x month)

What You'll Bring

Required:

• Bachelor's degree in life sciences or related field
• On site clinical monitoring experience (CRA): 1.5 years for CRA II, more than 3 years for Senior CRA
• Strong understanding of ICH-GCP guidelines and regulatory requirements
• Excellent communication and interpersonal skills
• Ability to work independently and manage multiple priorities
• Therapeutic area experience in Oncology
• Fluent in English + local language
• Location: Must be based in São Paulo or Rio de Janeiro, Brazil

Why Join Parexel?

• Career Growth: Comprehensive training programs and clear advancement pathways
• Global Impact: Work on innovative trials across diverse therapeutic areas
• Work-Life Balance: Flexible working arrangements
• Competitive Benefits: 100% employer-paid health insurance for you and your family, Meal voucher, internet
• Inclusive Culture: Join a diverse, collaborative team committed to excellence

Ready to Make a Difference?

Apply today and become part of a team that's transforming the future of healthcare.