Clinical Research Associate III (m/f/d) – Belgium / The Netherlands (Dutch speaking)
- Jotec GmbH Jobportal
- Kaufmännische Berufe (Sonstige)
- Publiziert: 28.05.2026
Your Strength
- 4+ years of experience in clinical research monitoring
- Strong knowledge of ISO 14155 GCP, MDR, FDA, and applicable regulatory requirements
- Experience managing clinical trial sites from study start-up through close-out
- Ability to work independently and manage multiple sites simultaneously
- Strong communication and relationship-building skills with investigators and site staff
- Excellent organizational, documentation, and problem-solving skills
- Willingness to travel for monitoring visits and site support activities
Your Contribution
- Manage 10–15 clinical study sites from start-up to closure
- Conduct monitoring visits in accordance with study protocols and regulatory requirements
- Build strong relationships with investigators and study coordinators
- Train sites on study procedures, data collection, and safety reporting
- Perform study initiation, maintenance, and close-out visits
- Review clinical data and support patient safety oversight
- Prepare monitoring reports, follow-up letters, and tracking updates
- Support audits, inspections, CAPA activities, and process improvements
- Mentor junior CRA team members and support training initiatives
- Collaborate cross-functionally with Clinical Affairs, QA/RA, R&D, Marketing, and external partners
Our Strength
- A mission-driven company focused on saving lives
- International and collaborative MedTech environment
- Hybrid working model with flexibility
- Opportunities for growth and professional development
- Innovative products and meaningful clinical impact
Contact
JOTEC GmbH, a wholly owned subsidiary of Artivion, Inc.,
Lotzenäcker 23, 72379 Hechingen
www.artivion.com