Clinical Research Associate - Monitoring Experience Required

Descripción del trabajo

At Artivion, we manufacture high-quality products and solutions for the treatment of aortic diseases. Asegúrese de inscribirse rápido, ya que se espera un gran volumen de solicitudes. We are hiring a Clinical Research Associate III - Home-Base 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

We look forward to receiving your application documents in English through our online application system.