Clinical Research Associate (Cra) Spain

CliniRx Research Private Limited; Alcobendas; Presencial; EUR 42.000 - 60.000; Jornada completa

Descripción de la vacante

Clinirx, a global full-service CRO, seeks a Clinical Research Associate (CRA) in Spain to join a fast-paced, globally connected team in Madrid. You will support site management, monitoring activities, and regulatory documentation for trials across phases, ensuring ethics and patient safety are upheld.

The role requires strong English and native Spanish, with excellent communication and problem-solving skills to thrive in a dynamic, cross-functional environment.

Formación

• Proven experience as a CRA in Spain.
• Strong knowledge of ICH-GCP guidelines and local regulations.
• Experience with site management, monitoring, initiation, and close-out visits.
• Ability to identify risks and implement mitigations.
• Excellent communication and organizational skills.
• Fluent in English and native Spanish required.

Responsabilidades

• Lead site management and monitoring activities.
• Coordinate site initiation, routine monitoring, and close-out visits.
• Prepare regulatory and Ethics Committee documentation.
• Maintain investigator/site relationships.
• Identify risks and implement mitigation strategies.
• Collaborate with global teams in fast-paced environments.

Conocimientos

CRA experience

ICH-GCP knowledge

Regulatory docs

Site management

Monitoring visits

Stakeholder mgmt

English fluency

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.

Clinical Research Associate (CRA) SPAIN • Madrid, Community of Madrid, Spain, Spain