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 Belgium
Your strength:
* 18 months to 4 years of site monitoring experience in clinical research
* Ability to work independently with limited supervision
* Excellent understanding of GCP, ISO 14155, MDR, FDA, EU, and local clinical regulations
* Strong communication and relationship-building skills with investigators and site personnel
* Proficiency in documentation, reporting, and data review processes
* Fluent in Dutch and English; additional language skills are an asset
* Organized, proactive, and detail-oriented approach
* Familiarity with electronic data capture systems and remote monitoring tools
Your contribution:
* Manage 10–15 clinical study sites (class 2–3 devices) from start-up to close-out
* Conduct and independently manage site monitoring visits (on-site and remote)
* Act as main point of contact between sites, sponsors, and stakeholders
* Review and verify clinical data and source documents for accuracy and compliance
* Prepare site visit reports, follow-up on action items, and maintain study documentation
* Conduct site selection, initiation, and close-out visits
* Support execution of clinical study protocols and ensure adherence to regulatory requirements
* Participate in quality assurance activities, audits, CAPAs, and training sessions
* Mentor and guide junior CRAs and assist in coordination of project-related tasks
* Ensure accurate and timely data transmission and DCF resolution
* Collaborate cross-functionally with Clinical Affairs, RA/QA, R&D, and external vendors
Our strength:
* A mission-driven and international Clinical Affairs team
* Diverse and impactful projects in the cardiovascular device space
* A structured onboarding process and professional development support
* Hybrid work flexibility and attractive benefits including pension plan and EGYM Wellpass
* Collaborative culture and strong clinical partnerships across EMEA
Apply 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