Senior Clinical Research Associate — Remote Spain

Artivion Emea; Arbo; Híbrido; EUR 55.000 - 75.000; Jornada completa

Descripción de la vacante

Artivion Emea seeks a Clinical Research Associate III for a home-based position in Spain. You will monitor sites, initiate and close studies, and ensure patient safety and data integrity across trials.

The ideal candidate has at least 4 years of advanced CRA experience, deep knowledge of GCP and regulatory requirements, and strong communication in English and Spanish. Catalan is a plus, cross-border monitoring possible near the Spain/France border.

Formación

• Minimum of 4 years of advanced experience in clinical research monitoring.
• In-depth knowledge of guidelines related to clinical trials involving human subjects (GCP) and regulatory requirements.
• Ability to mentor junior team members and collaborate with cross-functional teams.
• Hands-on experience with monitoring systems, source data verification, and compliance tracking.
• Fluent communication in English and Spanish; Catalan preferred; French cross-border considerations.

Responsabilidades

• Independently manage all phases of clinical trial site activities, including site identification, initiation, monitoring, and close-out.
• Conduct monitoring visits in accordance with study protocols, GCP, and applicable regulatory requirements.
• Perform source data verification and data review to ensure patient safety, protocol compliance, and data integrity.
• Conduct site training, initiation visits, and support audit and inspection readiness.
• Collaborate closely with Clinical Operations, Data Management, Medical Affairs, and other cross-functional teams.
• Support investigator meetings, coordinator meetings, and deliver presentations or training sessions when required.
• Mentor junior CRAs and contribute to process improvements and best practices.
• Participate in CAPA activities, quality initiatives, audits, and continuous improvement efforts.

Conocimientos

Clinical research monitoring

Regulatory knowledge

Collaboration & mentorship

Source data verification

English & Spanish fluency

Descripción del empleo

Artivion Emea seeks a Clinical Research Associate III for a home-based position in Spain. You will monitor sites, initiate and close studies, and ensure patient safety and data integrity across trials.

The ideal candidate has at least 4 years of advanced CRA experience, deep knowledge of GCP and regulatory requirements, and strong communication in English and Spanish. Catalan is a plus, cross-border monitoring possible near the Spain/France border.