Cra - Clinical Research Associate Sponsor Dedicated Team Czech Republic

IQVIA UK

Czech Republic
Ich-gcp guidelines
Patient recruitment support
Rca and capa management
Performing visits (such as selection, initiation, monitoring and close-out) according to ICH-GCP guidelines

Job Summary

  • Performing visits (such as selection, initiation, monitoring and close-out) according to ICH-GCP guidelines.
  • Management and archiving of study documents in eTMF.
  • IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry.

Matching Summary

Performing visits (such as selection, initiation, monitoring and close-out) according to ICH-GCP guidelines.

Skills & Requirements

Must-have

  • ICH-GCP guidelines
  • patient recruitment support
  • RCA and CAPA management
  • eTMF document management
  • travel across the country
  • driving license

Nice-to-have

  • passion for science
  • helping patients
  • collaborating with sites
  • diversity and inclusion advocate

Key Requirements

  • MSc and/or BSc education level
  • Proficient Czech and English
  • Minimum 1 year CRA experience
  • CTMS, eTMF, EDC systems experience
  • Experience in different studies, phases, visits, indications

Work Rights

Not specified

Tailored Resume

Cover Letter