335 Best Full-time Educación Jobs in Alcantarilla (July 2026)

Clinical Research Associate Iii

3 days ago

Murcia

ppIt’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. Your contribution as a Clinical Research Associate III – Home‑Based in Spain is essential to our mission. /p h3Key Requirements /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 liFluent communication in English and Spanish (Catalan is preferred), French optional /li /ul h3Key Responsibilities /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 /li liCollaborate 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 h3About the Role /h3 ul liBased in Spain (candidates from France may be considered in case a candidate lives nearby the Spain/France border and is eager to do cross‑border monitoring) /li liHybrid working model with flexibility /li /ul h3Why Join Us /h3 ul liA mission‑driven company focused on saving lives /li liInternational and collaborative MedTech environment /li liOpportunities for growth and professional development /li liInnovative products and meaningful clinical impact /li /ul pContact: Brian Russo, JOTEC GmbH, a wholly owned subsidiary of Artivion, Inc., Lotzenäcker 23, 72379 Hechingen. /p /p #J-18808-Ljbffr

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