Clinical Research Associate III
1 day ago
Santiago de Compostela
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.brWe are hiring abrClinical Research Associate III – Home-Based in Spain (Spanish speaking candidates in France are also welcome)brYour StrengthbrMinimum of 4 years of advanced experience in clinical research monitoringbrIn-depth knowledge of regulations and guidelines related to clinical trials involving human subjects (e.g., ISO 14155, GCP, MDR, EU, FDA)brAbility to independently manage 10–15 study sites from start-up through close-outbrExcellent communication skills for site interaction, training, and issue resolutionbrStrong collaboration and mentorship abilities, with a passion for supporting and guiding junior team membersbrHands-on experience with monitoring systems, source data verification, and compliance trackingbrStrong organizational skills with the ability to manage multiple priorities in a dynamic environmentbrWillingness to travel regularly for site visits and investigator meetings across France and SpainbrBased 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)brFluent communication in English and Spanish (Catalan is preferred, French optional)brYour ContributionbrIndependently manage all phases of clinical trial site activities, including site identification, initiation, monitoring, and close-outbrConduct monitoring visits in accordance with study protocols, GCP, and applicable regulatory requirementsbrAct as the primary contact for investigational sites, ensuring compliance and providing ongoing supportbrBuild and maintain strong relationships with investigators, study coordinators, and site personnelbrIdentify study risks, recommend solutions, and ensure timely resolution of site-related issuesbrPerform source data verification and data review to ensure patient safety, protocol compliance, and data integritybrConduct site training, initiation visits, and support audit and inspection readinessbrCollaborate closely with Clinical Operations, Data Management, Medical Affairs, and other cross-functional teamsbrSupport investigator meetings, coordinator meetings, and deliver presentations or training sessions when requiredbrMentor junior CRAs and contribute to process improvements and best practicesbrParticipate in CAPA activities, quality initiatives, audits, and continuous improvement effortsbrOur StrengthbrA mission-driven company focused on saving livesbrInternational and collaborative MedTech environmentbrHybrid working model with flexibilitybrOpportunities for growth and professional developmentbrInnovative products and meaningful clinical impactbrContactbrApply now and join the Artivion team. We look forward to receiving your application documents in English through our online application system.brBrian RussobrT:brJOTEC GmbH, a wholly owned subsidiary of Artivion, Inc.brLotzenäcker 23, 72379 Hechingen