Site Management Intern

IQVIA

Sofia, Bulgaria
Clinical research
Ich-gcp principles
Study operations
Participate in a structured onboarding program covering Clinical Research, ICH-GCP, clinical monitoring principles, and study operations

Job Summary

  • Participate in a structured onboarding program covering Clinical Research, ICH-GCP, clinical monitoring principles, and study operations.
  • Shadow experienced CRAs and CTAs to observe daily responsibilities and decision-making in real study environments.
  • Assist with eTMF filing, document QC checks, and maintenance of trial trackers.

Matching Summary

Participate in a structured onboarding program covering Clinical Research, ICH-GCP, clinical monitoring principles, and study operations.

Skills & Requirements

Must-have

  • Clinical Research
  • ICH-GCP principles
  • study operations
  • site monitoring
  • eTMF filing
  • clinical systems

Nice-to-have

  • eager to begin a career
  • hands-on exposure
  • fresh ideas
  • process optimization

Key Requirements

  • Student status
  • Eagerness to learn clinical research

Work Rights

Not specified

Tailored Resume

Cover Letter