Clinical Research Associate II (m/f/d) – Belgium

Clinical Research Associate II (m/f/d) – Belgium

Join to apply for the Clinical Research Associate II (m/f/d) – Belgium role at Artivion EMEA.

At Artivion, we manufacture high‑quality products and solutions for the treatment of aortic diseases. Together with surgeons worldwide, we save lives. As an important link in the chain, you make a contribution to saving lives together with us.

Qualifications

• 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

Responsibilities

• 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

Benefits

• 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

Contact

Apply now and join the Artivion Team. We are looking forward to receiving your application documents in English directly via our online system. Brian Russo, T: +41 435 08 39 01
JOTEC GmbH, a wholly owned subsidiary of Artivion, Inc.,
Lotzenäcker 23, 72379 Hechingen
www.artivion.com