Clinical Research Associate II and Senior
Primary Location: Brazil, Sao Paulo ID de la oferta R0000038161 Categoría Clinical Trials Fecha de publicación 01/21/2026Overview
Como Auxiliar de investigación clínica (CRA) en Parexel, usted cumple una función vital para hacerles llegar los tratamientos a los pacientes con mayor rapidez. La prioridad de nuestros CRA es la seguridad y el bienestar de los pacientes. Cuando viaje a centros de investigación y cumpla sus obligaciones de monitoreo, lo alentamos a ser inquisitivo, a asumir responsabilidades, a construir relaciones y a actuar con integridad.
Únase a un equipo con una gran variedad de experiencias y conocimientos y trabaje en proyectos globales dentro de una amplia gama de áreas terapéuticas. Estamos buscando personas que deseen crecer en el ámbito personal y profesional y que respalden a sus colegas de manera global y multidisciplinaria.
Perfil del éxito
¿Posee estas competencias sociales y rasgos interpersonales para tener éxito en Parexel?
- Comunicador
- Organizado
- Contratos laborales flexibles
- Emprendedor
- Orientado al detalle
- Solucionador de problemas
Acerca de este rol
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 astrategic partnerand 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.
POTENCIAL TRAYECTORIA PROFESIONAL
Parexel ofrece diversas trayectorias profesionales y programas de desarrollo interno para que los CRA avancen al próximo nivel. Esto podría incluir mejorar su puesto técnico, transferencia a gerencia o cambiar a otras áreas del negocio.
- APEX CRA
- CRA I
- CRA II
- CRA Sénior
- Gestión de ProyectosExperto en la MateriaGestión de Proyectos
Perspectivas de los empleados
nuestro equipo
POR QUÉ TRABAJAR EN PAREXEL
