Centralized Monitoring Assistant

IQVIA

Onsite
2 years work experience minimum
6 months relevant clinical experience
Microsoft excel word powerpoint skills
The role provides study level administrative support to the clinical study management team under supervision

Job Summary

  • The role provides study level administrative support to the clinical study management team under supervision.
  • The incumbent is responsible for periodic review of site-level KRIs and facilitating early identification of risks.
  • IQVIA is a leading global provider of clinical research services committed to integrity in its hiring process.

Matching Summary

The role provides study level administrative support to the clinical study management team under supervision.

Skills & Requirements

Must-have

  • 2 years work experience minimum
  • 6 months relevant clinical experience
  • Microsoft Excel Word PowerPoint skills
  • Good Clinical Practice knowledge
  • Strong communication and time management

Nice-to-have

  • Detail-oriented approach to work delivery
  • Ability to establish effective working relationships
  • Experience with site performance reviews

Key Requirements

  • Minimum 2 years work experience
  • Minimum 6 months relevant experience
  • Graduate or Post Graduate in Life Sciences
  • Basic knowledge of ICH-GCP regulations

Work Rights

Not specified

Tailored Resume

Cover Letter