When our values align theres no limit to what we can achieve.

At Parexel we all share the same goal - to improve the worlds 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 were 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 youll be more than a monitoryoull be astrategic partnerand the primary point of contact for clinical sites throughout the entire trial lifecycle. From site identification through close-out youll 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 youll combine relationship management strategic thinking and regulatory expertise to drive sites to peak performance.

What Youll 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 Youll Bring

Required:

• Bachelors 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 thats transforming the future of healthcare.