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Clinical Research Associate; CRA

Trabajo disponible en: 04810, Madrid, Andalucia, España
Empresa: CliniRx
Tiempo completo puesto
Publicado en 2026-09-18
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

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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.

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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.
Requisitos del puesto
10+ años Experiencia laboral
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