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ARArtivion

Clinical Research Associate III(m/w/x)

Hechingen
Full-timeWith Home OfficeExperienced

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

  • EnglishBusiness 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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