Clinical Research Associate 2/ Sr Cra1 - Based In Slovakia

IQVIA Inc

Slovakia
Site selection and monitoring
Subject recruitment planning
Quality and integrity evaluation
Performing site selection, initiation, monitoring and close-out visits

Job Summary

  • Performing site selection, initiation, monitoring and close-out visits.
  • Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelines.
  • Resources that promote your career growth, leaders that support flexible work schedules, and programs to help you build your therapeutic knowledge.

Matching Summary

Performing site selection, initiation, monitoring and close-out visits.

Skills & Requirements

Must-have

  • site selection and monitoring
  • subject recruitment planning
  • quality and integrity evaluation
  • regulatory requirements management
  • tracking submissions and data queries
  • collaboration with site experts and clients

Nice-to-have

  • career growth resources
  • supportive leadership
  • therapeutic knowledge building
  • excellent working environment

Key Requirements

  • University degree in scientific discipline or health care
  • At least 2 years of experience as a Clinical Research Associate
  • Very good computer skills including MS Office
  • Excellent command of Slovak and English language
  • Driver’s license class B

Work Rights

Not specified

Tailored Resume

Cover Letter