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Clinical Research Associate; CRA

Trabajo disponible en: 04810, Madrid, Andalucia, España
Empresa: CliniRx
Tiempo completo puesto
Publicado en 2026-09-12
Especializaciones laborales:
  • Servicios Médicos
    Investigación clínica
  • Investigación/Desarrollo
    Investigación clínica
Descripción del trabajo
Puesto: Clinical Research Associate (CRA
Clinirx, a global full-service Clinical Research Organization (CRO), is expanding its operations and we are currently seeking experienced professionals to join our growing team in Spain.

Position
Clinical Research Associate (CRA) Spain

Location:

Spain
At Clinirx, we partner with pharmaceutical, biotechnology, and medical device companies worldwide, providing expertise across all phases of clinical development. Our mission is to advance innovative therapies while maintaining the highest standards of compliance, ethics, and patient safety.

What We Are Looking For
Proven experience working as a CRA in Spain
Strong knowledge of ICH-GCP guidelines and local clinical research regulations
Hands-on experience with:
Site management and monitoring activities
Site initiation, routine monitoring, and close-out visits
Regulatory and Ethics Committee documentation
Investigator/site relationship management
Ability to proactively identify risks and implement mitigation strategies
Strong sense of urgency, accountability, and ownership
Excellent communication, organizational, and problem-solving skills
Strong stakeholder management and cross-functional collaboration abilities
Ability to work effectively in fast-paced global environments
Spanish (mother tongue - proficiency) and fluent English (written and verbal) are required.

Why Join Clinirx?
At Clinirx, you will become part of a collaborative and globally connected team committed to:
Excellence in clinical research
Innovation and continuous improvement
Ethical conduct and regulatory compliance
Accelerating access to innovative therapies for patients worldwide
This is an exciting opportunity to contribute strategically to clinical trial activation and regulatory excellence in EU.

For additional details or to apply directly:
Requisitos del puesto
10+ años Experiencia laboral
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