Clinical Research Associate 1/2 - Czech Republic

IQVIA

Prague, Czech Republic
Site selection and monitoring
Regulatory requirements adherence
Good clinical practice
Perform site selection, initiation, monitoring and close-out visits to ensure quality and integrity of site practices

Job Summary

  • Perform site selection, initiation, monitoring and close-out visits to ensure quality and integrity of site practices.
  • Manage progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions.
  • IQVIA offers resources for career growth, supportive leaders, programs to build therapeutic knowledge, and an excellent working environment.

Matching Summary

Perform site selection, initiation, monitoring and close-out visits to ensure quality and integrity of site practices.

Skills & Requirements

Must-have

  • site selection and monitoring
  • regulatory requirements adherence
  • Good Clinical Practice
  • International Conference on Harmonization
  • tracking submissions and recruitment
  • Czech and English language proficiency

Nice-to-have

  • career growth resources
  • flexible work schedules
  • therapeutic knowledge building
  • effective working relationships

Key Requirements

  • University degree in scientific discipline
  • Experience in Pharma Industry
  • Experience in Clinical Trials environment
  • Very good computer skills including MS Office
  • Flexibility to travel
  • Driver’s license class B

Work Rights

Not specified

Tailored Resume

Cover Letter