Experienced Clinical Research Associate (m/w/d), Multi-sponsor, Germany

IQVIA

Frankfurt, Germany
Clinical trial monitoring
Gcp and ich guidelines
Site selection and initiation
You will perform site selection, initiation, monitoring and close-out visits, and support the development of a subject recruitment plan

Job Summary

  • You will perform site selection, initiation, monitoring and close-out visits, and support the development of a subject recruitment plan.
  • This role involves evaluating site practices for quality and integrity in accordance with regulatory requirements like GCP and ICH guidelines.
  • IQVIA offers resources for career growth, flexible work schedules, therapeutic knowledge programs, and dynamic work environments.

Matching Summary

You will perform site selection, initiation, monitoring and close-out visits, and support the development of a subject recruitment plan.

Skills & Requirements

Must-have

  • Clinical trial monitoring
  • GCP and ICH guidelines
  • Site selection and initiation
  • Subject recruitment planning
  • German and English language proficiency

Nice-to-have

  • Building investigator relationships
  • Dynamic work environments
  • Career growth resources

Key Requirements

  • Minimum two years on-site monitoring experience
  • University Degree in life science or scientific discipline or healthcare apprenticeship
  • Knowledge of GCP and ICH guidelines
  • Flexibility for up to 60% business travel
  • Driver's license class B

Work Rights

Not specified

Tailored Resume

Cover Letter