Experienced Clinical Research Associate- Israel

IQVIA Inc

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

Job Summary

  • The role involves performing site monitoring visits to ensure studies are conducted according to the protocol and applicable regulations.
  • Candidates must work with sites to adapt and drive subject recruitment plans while maintaining high standards of data integrity.
  • The position requires managing regulatory submissions, enrollment tracking, and ensuring proper documentation is filed in the Trial Master File.

Matching Summary

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

Skills & Requirements

Must-have

  • Good Clinical Practice (GCP) knowledge
  • International Conference on Harmonization (ICH) guidelines
  • Site monitoring visit execution
  • Subject recruitment plan management
  • Trial Master File maintenance

Nice-to-have

  • Strong organizational skills
  • Effective time management abilities
  • Problem-solving capabilities
  • Excellent verbal communication in English

Key Requirements

  • At least 2 years of on-site monitoring experience
  • High School Diploma or equivalent Degree in scientific discipline
  • Proficiency in Microsoft Word, Excel, and PowerPoint

Work Rights

Not specified

Tailored Resume

Cover Letter