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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.
Requirements
- 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
Tasks
- 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
Work Experience
- 4 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
Benefits
Flexible Working
- Hybrid working model with flexibility
Career Advancement
- Opportunities for growth and professional development
Startup Environment
- Innovative products
Purpose-Driven Work
- 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.
Requirements
- 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
Tasks
- 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
Work Experience
- 4 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
Benefits
Flexible Working
- Hybrid working model with flexibility
Career Advancement
- Opportunities for growth and professional development
Startup Environment
- Innovative products
Purpose-Driven Work
- Meaningful clinical impact
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
Artivion
Industry
Healthcare
Description
Das Unternehmen stellt hochwertige Produkte und Lösungen zur Behandlung von Aortenerkrankungen her.
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