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

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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 regu

📌 Clinical Research Associate III (Arbo)
🏢 Artivion EMEA
📍 Arbo