Buscar empleo: 142 ofertas de trabajo de Educación en Meaño (julio 2026)

Clinical Research Associate Iii

hace 6 horas

Marín

p 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. /pbr /Solicitar este puesto es sencillo. Desplácese hacia abajo y haga clic en "Solicitar" para ser considerado para esta posición.br /pb We are hiring a /b /ppb Clinical Research Associate III – Home-Based in Spain (Spanish speaking candidates in France are also welcome) /b /p pb Your Strength /b /p ulli Minimum of 4 years of advanced experience in clinical research monitoring /lili In-depth knowledge of regulations and guidelines related to clinical trials involving human subjects (e.G., ISO 14155, GCP, MDR, EU, FDA) /lili Ability to independently manage 10–15 study sites from start-up through close-out /lili Excellent communication skills for site interaction, training, and issue resolution /lili Strong collaboration and mentorship abilities, with a passion for supporting and guiding junior team members /lili Hands-on experience with monitoring systems, source data verification, and compliance tracking /lili Strong organizational skills with the ability to manage multiple priorities in a dynamic environment /lili Willingness to travel regularly for site visits and investigator meetings across France and Spain /lili 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) /lili Fluent communication in English and Spanish (Catalan is preferred, French optional) /li /ul pb Your Contribution /b /pulli Independently manage all phases of clinical trial site activities, including site identification, initiation, monitoring, and close-out /lili Conduct monitoring visits in accordance with study protocols, GCP, and applicable regulatory requirements /lili Act as the primary contact for investigational sites, ensuring compliance and providing ongoing support /lili Build and maintain strong relationships with investigators, study coordinators, and site personnel /lili Identify study risks, recommend solutions, and ensure timely resolution of site-related issues /lili Perform source data verification and data review to ensure patient safety, protocol compliance, and data integrity /lili Conduct site training, initiation visits, and support audit and inspection readiness /lili Collaborate closely with Clinical Operations, Data Management, Medical Affairs, and other cross-functional teams /lili Support investigator meetings, coordinator meetings, and deliver presentations or training sessions when required /lili Mentor junior CRAs and contribute to process improvements and best practices /lili Participate in CAPA activities, quality initiatives, audits, and continuous improvement efforts /li /ul pb Our Strength /b /p ulli A mission-driven company focused on saving lives /lili International and collaborative MedTech environment /lili Hybrid working model with flexibility /lili Opportunities for growth and professional development /lili Innovative products and meaningful clinical impact /li /ul pb Contact /b /pp Apply now and join the Artivion team. xhfqzwm We look forward to receiving your application documents in strong English /strong through our online application system. /ppb Brian Russo /b /p p T: /pp JOTEC GmbH, a wholly owned subsidiary of Artivion, Inc. /pp Lotzenäcker 23, 72379 Hechingen /p

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