Overview
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
At Parexel, we are a leading Clinical Research Organization (CRO) specializing in delivering life‑changing medicines to patients. We are seeking an experienced Clinical Research Associate II/Sr to join our team. As a CRA, you’ll be joining a fast‑paced, driven environment that’s helping to make a life‑changing difference to patients by ensuring high‑quality clinical trial execution, building strong site partnerships, and maintaining compliance across all phases of a study. Through the collaboration and diversity of our teams, CRAs are provided with multiple opportunities to excel and discover where their skills can take them.
Who We’re Looking For
Detail‑oriented and a strong problem solver
Highly communicative, collaborative, and adaptable
Motivated, accountable, and able to work independently
Positive, professional, and comfortable supporting virtual and in‑person teams
What You’ll Do
Monitor clinical trial sites through on‑site and remote visits
Build and maintain strong relationships with investigators and site staff
Collaborate with cross‑functional teams to meet project timelines
Manage site‑level study documentation, systems updates, and visit reports
Implement corrective actions when needed to maintain study integrity
Ensure sites are always audit- and inspection-ready
Additional Details
Home‑based role; preference for candidates residing in Mexico City
Must be fluent in English and Spanish
Bachelor’s degree in life sciences, pharmacy, nursing, or related field is required
A minimum of 1 year of CRA experience monitoring oncology trials is required
Must be able to travel and hold a valid driver’s license
Why Join Us
Be part of groundbreaking projects pushing the boundaries of clinical research
Work in a collaborative and inclusive environment that values your expertise
Unlock career growth and professional development opportunities
Enjoy work‑life balance and flexible working arrangements
If this job doesn’t sound like your next step, but you know someone who’d be a perfect fit, feel free to share this opportunity with them!
At Parexel, we embrace flexibility and understand the importance of balancing your career with your personal life. Come join us where learning is constant and you’re exposed to a world of experiences and open doors.
#LI-REMOTE
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
