Clinical Research Associate II

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. Contribute your strengths and let us grow together.We are hiring Clinical Research Associate II (m/f/d) – The Netherlands or BelgiumYour strength:18 months to 4 years of site monitoring experience in clinical researchAbility to work independently with limited supervisionExcellent understanding of GCP, ISO 14155, MDR, FDA, EU, and local clinical regulationsStrong communication and relationship-building skills with investigators and site personnelProficiency in documentation, reporting, and data review processesFluent in Dutch and English; additional language skills are an assetOrganized, proactive, and detail-oriented approachFamiliarity with electronic data capture systems and remote monitoring toolsYour contribution:Manage 10–15 clinical study sites (class 2–3 devices) from start-up to close-outConduct and independently manage site monitoring visits (on-site and remote)Act as main point of contact between sites, sponsors, and stakeholdersReview and verify clinical data and source documents for accuracy and compliancePrepare site visit reports, follow-up on action items, and maintain study documentationConduct site selection, initiation, and close-out visitsSupport execution of clinical study protocols and ensure adherence to regulatory requirementsParticipate in quality assurance activities, audits, CAPAs, and training sessionsMentor and guide junior CRAs and assist in coordination of project-related tasksEnsure accurate and timely data transmission and DCF resolutionCollaborate cross-functionally with Clinical Affairs, RA/QA, R&D, and external vendorsOur strength:A mission-driven and international Clinical Affairs teamDiverse and impactful projects in the cardiovascular device spaceA structured onboarding process and professional development supportHybrid work flexibility and attractive benefits including pension plan and EGYM WellpassCollaborative culture and strong clinical partnerships across EMEAApply now and become part of the Artivion team. We look forward to receiving your application documents in English.Contact: Brian Russo – T: +41 435 08 39 01 JOTEC GmbH, a wholly owned subsidiary of Artivion, Inc.www.artivion.com