Cra 1

IQVIA

Good clinical practice (gcp) guidelines
International conference on harmonization (ich)
Site monitoring visits execution
The role involves performing site monitoring visits to ensure studies are conducted according to protocol and regulations

Job Summary

  • The role involves performing site monitoring visits to ensure studies are conducted according to protocol and regulations.
  • Candidates must manage subject recruitment plans and maintain the Investigator's Site File in compliance with GCP/ICH guidelines.
  • The position requires evaluating site practices for quality and integrity while collaborating with study team members.

Matching Summary

The role involves performing site monitoring visits to ensure studies are conducted according to protocol and regulations.

Skills & Requirements

Must-have

  • Good Clinical Practice (GCP) guidelines
  • International Conference on Harmonization (ICH)
  • site monitoring visits execution
  • subject recruitment plan tracking
  • Trial Master File maintenance

Nice-to-have

  • strong problem-solving skills
  • effective time management abilities
  • excellent verbal communication skills

Key Requirements

  • Bachelor's Degree in scientific discipline or health care
  • Prior monitoring experience or CRA training program completion
  • Proficiency in Microsoft Word, Excel, and PowerPoint

Work Rights

Not specified

Tailored Resume

Cover Letter