ppClinical Research Associate III Artivion EMEA•Gijón, Asturias, ES /p pDescripción del trabajo /p pIt'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. /p h3We are hiring a /h3 pClinical Research Associate III – Home-Based in Spain (Spanish speaking candidates in France are also welcome) /p h3Your Strength /h3 ul liMinimum of 4 years of advanced experience in clinical research monitoring /li liIn-depth knowledge of regulations and guidelines related to clinical trials involving human subjects (e.g., ISO 14155, GCP, MDR, EU, FDA) /li liAbility to independently manage 10–15 study sites from start-up through close-out /li liExcellent communication skills for site interaction, training, and issue resolution /li liStrong collaboration and mentorship abilities, with a passion for supporting and guiding junior team members /li liHands-on experience with monitoring systems, source data verification, and compliance tracking /li liStrong organizational skills with the ability to manage multiple priorities in a dynamic environment /li liWillingness to travel regularly for site visits and investigator meetings across France and Spain /li liBased 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) /li liFluent communication in English and Spanish (Catalan is preferred, French optional)



/li /ul h3Your Contribution /h3 ul liIndependently manage all phases of clinical trial site activities, including site identification, initiation, monitoring, and close-out /li liConduct monitoring visits in accordance with study protocols, GCP, and applicable regulatory requirements /li liAct as the primary contact for investigational sites, ensuring compliance and providing ongoing support /li liBuild and maintain strong relationships with investigators, study coordinators, and site personnel /li liIdentify study risks, recommend solutions, and ensure timely resolution of site-related issues /li liPerform source data verification and data review to ensure patient safety, protocol compliance, and data integrity /li liConduct site training, initiation visits, and support audit and inspection readiness /liliCollaborate closely with Clinical Operations, Data Management, Medical Affairs, and other cross-functional teams /li liSupport investigator meetings, coordinator meetings, and deliver presentations or training sessions when required /li liMentor junior CRAs and contribute to process improvements and best practices /li liParticipate in CAPA activities, quality initiatives, audits, and continuous improvement efforts /li /ul h3Our Strength /h3 ul liA mission-driven company focused on saving lives /li liInternational and collaborative MedTech environment /li liHybrid working model with flexibility /li liOpportunities for growth and professional development /li liInnovative products and meaningful clinical impact /li /ul h3Contact /h3 pWe look forward to receiving your application documents in English through our online application system. /p pBrian Russo /p pT: /p pJOTEC GmbH, a wholly owned subsidiary of Artivion, Inc. /p pLotzenäcker 23, 72379 Hechingen /p pClinical Research Associate III • Gijón, Asturias, ES /p /p #J-18808-Ljbffr

📌 Clinical Research Associate Iii (Gijón)
🏢 Artivion EMEA
📍 Gijón