Dein persönlicher KI-Karriere-Agent
Clinical Research Associate III(m/w/x)
Monitoring 10-15 clinical study sites for aortic disease treatments, building investigator relationships. 4+ years clinical research monitoring experience required. Hybrid work, growth opportunities.
Anforderungen
- 4+ years clinical research monitoring experience
- Strong knowledge of ISO 14155 GCP, MDR, FDA
- Experience managing clinical trial sites
- Ability to work independently and manage multiple sites
- Strong communication and relationship-building skills
- Excellent organizational, documentation, and problem-solving skills
- Willingness to travel for monitoring visits
Aufgaben
- Manage 10–15 clinical study sites from start-up to closure
- Conduct monitoring visits according to study protocols and regulations
- 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
Berufserfahrung
- 4 Jahre
Ausbildung
- Bachelor-AbschlussODER
- Master-Abschluss
Sprachen
- Englisch – verhandlungssicher
Benefits
Flexibles Arbeiten
- Hybrid working model with flexibility
Karriere- und Weiterentwicklung
- Opportunities for growth and professional development
Startup-Atmosphäre
- Innovative products
Sinnstiftende Arbeit
- Meaningful clinical impact
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Clinical Research Associate III(m/w/x)
Monitoring 10-15 clinical study sites for aortic disease treatments, building investigator relationships. 4+ years clinical research monitoring experience required. Hybrid work, growth opportunities.
Anforderungen
- 4+ years clinical research monitoring experience
- Strong knowledge of ISO 14155 GCP, MDR, FDA
- Experience managing clinical trial sites
- Ability to work independently and manage multiple sites
- Strong communication and relationship-building skills
- Excellent organizational, documentation, and problem-solving skills
- Willingness to travel for monitoring visits
Aufgaben
- Manage 10–15 clinical study sites from start-up to closure
- Conduct monitoring visits according to study protocols and regulations
- 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
Berufserfahrung
- 4 Jahre
Ausbildung
- Bachelor-AbschlussODER
- Master-Abschluss
Sprachen
- Englisch – verhandlungssicher
Benefits
Flexibles Arbeiten
- Hybrid working model with flexibility
Karriere- und Weiterentwicklung
- Opportunities for growth and professional development
Startup-Atmosphäre
- Innovative products
Sinnstiftende Arbeit
- Meaningful clinical impact
Gefällt dir diese Stelle?
BetaDein Career Agent findet täglich ähnliche Jobs für dich.
Über das Unternehmen
Artivion
Branche
Healthcare
Beschreibung
Das Unternehmen stellt hochwertige Produkte und Lösungen zur Behandlung von Aortenerkrankungen her.
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