Clinical Research Associate (CRA) SPAIN

CliniRx; Madrid; Presencial; EUR 42.000 - 60.000; Jornada completa

Descripción de la vacante

Clinirx is expanding its clinical operations in Spain and seeks an experienced Clinical Research Associate to oversee site management and monitoring across trials. You will lead site initiation, monitoring visits, and close‑out activities, ensuring regulatory compliance and robust documentation.

The role requires strong ICH-GCP knowledge, excellent communication, and the ability to manage multiple sites in a fast-paced, global environment.

Formación

• 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 (native) and fluent English (written and verbal) are required.

Responsabilidades

• Oversee site management and monitoring activities.
• Coordinate site initiation, routine monitoring, and close‑out visits.
• Prepare and manage regulatory and Ethics Committee documentation.
• Foster investigator/site relationships and stakeholder collaboration.
• Identify risks and implement mitigation strategies to protect trial timelines.

Conocimientos

CRA experience

ICH-GCP knowledge

Site management

Monitoring visits

Regulatory documentation

Investigator relationships

Risk mitigation

Urgency & ownership

Communication skills

Organizational skills

Problem-solving

Spanish language

English proficiency

Stakeholder management

Cross-functional collaboration

Global environment adaptability

Descripción del empleo

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

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.

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.