Experienced Clinical Research Associate, Multi-sponsor, France

IQVIA UK

Paris, France
Hybrid
2 years clinical oncology experience
Good clinical practice (gcp) knowledge
Site monitoring visit execution
The role involves conducting clinical monitoring visits in accordance with study protocols and Good Clinical Practice guidelines

Job Summary

  • The role involves conducting clinical monitoring visits in accordance with study protocols and Good Clinical Practice guidelines.
  • Candidates must possess prior clinical oncology experience to effectively manage assigned studies and site expectations.
  • This position offers a flexible working arrangement that is either hybrid or home-based within major French cities.

Matching Summary

The role involves conducting clinical monitoring visits in accordance with study protocols and Good Clinical Practice guidelines.

Skills & Requirements

Must-have

  • 2 years clinical oncology experience
  • Good Clinical Practice (GCP) knowledge
  • Site monitoring visit execution
  • Trial Master File maintenance
  • Case Report Form management

Nice-to-have

  • Flexible hybrid or home-based work
  • Nationwide travel capability
  • Effective time and financial management
  • Strong problem-solving skills
  • Collaborative team relationship building

Key Requirements

  • Bachelor's Degree in scientific discipline
  • Prior 2 years clinical oncology experience
  • Advanced knowledge of GCP and ICH guidelines
  • Proficiency in Microsoft Office suite

Work Rights

Not specified

Tailored Resume

Cover Letter