Clinical Research Associate Iii
hace 3 horas
Foz
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. /ppWe are hiring abr /Por favor, presente su candidatura sin demora si su perfil encaja bien con este puesto, debido al alto nivel de interés.br /Clinical Research Associate III – Home-Based in Spain (Spanish speaking candidates in France are also welcome) /ppYour Strength /ppMinimum of 4 years of advanced experience in clinical research monitoringbr /In-depth knowledge of regulations and guidelines related to clinical trials involving human subjects (e.G., ISO 14155, GCP, MDR, EU, FDA)br /Ability to independently manage 10–15 study sites from start-up through close-outbr /Excellent communication skills for site interaction, training, and issue resolutionbr /Strong collaboration and mentorship abilities, with a passion for supporting and guiding junior team membersbr /Hands-on experience with monitoring systems, source data verification, and compliance trackingbr /Strong organizational skills with the ability to manage multiple priorities in a dynamic environmentbr /Willingness to travel regularly for site visits and investigator meetings across France and Spainbr /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)br /Fluent communication in English and Spanish (Catalan is preferred, French optional) /ppYour Contributionbr /Independently manage all phases of clinical trial site activities, including site identification, initiation, monitoring, and close-outbr /Conduct monitoring visits in accordance with study protocols, GCP, and applicable regulatory requirementsbr /Act as the primary contact for investigational sites, ensuring compliance and providing ongoing supportbr /Build and maintain strong relationships with investigators, study coordinators, and site personnelbr /Identify study risks, recommend solutions, and ensure timely resolution of site-related issuesbr /Perform source data verification and data review to ensure patient safety, protocol compliance, and data integritybr /Conduct site training, initiation visits, and support audit and inspection readinessbr /Collaborate closely with Clinical Operations, Data Management, Medical Affairs, and other cross-functional teamsbr /Support investigator meetings, coordinator meetings, and deliver presentations or training sessions when requiredbr /Mentor junior CRAs and contribute to process improvements and best practicesbr /Participate in CAPA activities, quality initiatives, audits, and continuous improvement efforts /ppOur Strength /ppA mission-driven company focused on saving livesbr /International and collaborative MedTech environmentbr /Hybrid working model with flexibilitybr /Opportunities for growth and professional developmentbr /Innovative products and meaningful clinical impact /ppContactbr /Apply now and join the Artivion team. xhfqzwm We look forward to receiving your application documents in /ppEnglish /ppthrough our online application system.br /Brian Russo /ppT: br /JOTEC GmbH, a wholly owned subsidiary of Artivion, Inc.br /Lotzenäcker 23, 72379 Hechingenbr / /p