Clinical Research Associate III

Artivion EMEA; España; Híbrido; EUR 60.000 - 95.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Hybrid working model

Opportunities for growth

Descripción de la vacante

Artivion is seeking a Clinical Research Associate III — Home-Based in Spain. You will independently manage site activities across Spain and neighboring regions, monitor visits per protocol and regulatory standards, and serve as the main liaison for investigators.

Fluency in English and Spanish is required, with Catalan preferred. This role offers hybrid flexibility and opportunities for professional growth.

Formación

• 4+ years in clinical research monitoring.
• Knowledge of ISO 14155, GCP, MDR, EU and FDA requirements.
• Ability to independently manage 10–15 study sites from start-up to close-out.
• Excellent communication for site interaction, training and issue resolution.
• Willingness to travel regularly for site visits.

Responsabilidades

• Manage all phases of site activities from start-up to close-out.
• Conduct monitoring visits per study protocol, GCP and regulatory requirements.
• Act as the primary contact for investigational sites, ensuring compliance and ongoing support.
• Build and maintain relationships with investigators, study coordinators and site personnel.
• Identify study risks and ensure timely resolution of site-related issues.
• Perform source data verification and data review to ensure patient safety and data integrity.
• Conduct site training, initiation visits, and support audits/inspections.
• Collaborate with Clinical Operations, Data Management, Medical Affairs and cross-functional teams.
• Support investigator meetings and deliver trainings when required.
• Mentor junior CRAs and contribute to process improvements.

Conocimientos

Clinical monitoring

GCP & regulation

Site management

Mentoring

Communication

Educación

Bachelor’s in Life Sciences

Herramientas

Monitoring systems

Source data verification

Compliance tracking

Descripción del empleo

It's a good feeling to know you're doing your best with purpose every day. At Artivion, we manufacture high-quality products and solutions for the treatment of aortic diseases. Together with surgeons worldwide, we save lives. In doing so, we rely on the strengths of each and every employee. Your strength counts, too: As an important link in the chain, you make a contribution to saving lives together with us. Bring your strengths and let us grow together.

We are hiring a

Clinical Research Associate III – Home-Based in Spain (Spanish speaking candidates in France are also welcome)

Your Strength

• Minimum of 4 years of advanced experience in clinical research monitoring
• In-depth knowledge of regulations and guidelines related to clinical trials involving human subjects (e.g., ISO 14155, GCP, MDR, EU, FDA)
• Ability to independently manage 10–15 study sites from start-up through close-out
• Excellent communication skills for site interaction, training, and issue resolution
• Strong collaboration and mentorship abilities, with a passion for supporting and guiding junior team members
• Hands-on experience with monitoring systems, source data verification, and compliance tracking
• Strong organizational skills with the ability to manage multiple priorities in a dynamic environment
• Willingness to travel regularly for site visits and investigator meetings across France and Spain
• Based in Spain (candidates from France may be considered in case a candidate lives nearby the Spain/France border and eager to do cross border monitoring)
• Fluent communication in English and Spanish (Catalan is preferred, French optional)

Your Contribution

• 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
• Act as the primary contact for investigational sites, ensuring compliance and providing ongoing support
• Build and maintain strong relationships with investigators, study coordinators, and site personnel
• Identify study risks, recommend solutions, and ensure timely resolution of site-related issues
• 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

Our Strength

• A mission-driven company focused on saving lives
• International and collaborative MedTech environment
• Hybrid working model with flexibility
• Opportunities for growth and professional development
• Innovative products and meaningful clinical impact

Contact

Brian Russo

T: [phone]

JOTEC GmbH, a wholly owned subsidiary of Artivion, Inc.