Centralized Monitoring Assistant

IQVIA

Multiple Locations
Onsite
Study level administrative support
System report generation
Tracking compliance
Under supervision, provides study level administrative support to the clinical study management team, including running system reports and preparing status reports

Job Summary

  • Under supervision, provides study level administrative support to the clinical study management team, including running system reports and preparing status reports.
  • Assists in updating and maintaining systems, driving tracking compliance to enable credible data for analysis.
  • Monitors site performance, identifies risks, and makes recommendations for corrective actions, reviewing their effectiveness.

Matching Summary

Under supervision, provides study level administrative support to the clinical study management team, including running system reports and preparing status reports.

Skills & Requirements

Must-have

  • study level administrative support
  • system report generation
  • tracking compliance
  • access management tasks
  • site level KRI review
  • site performance monitoring

Nice-to-have

  • effective time management
  • results and detail-oriented
  • establish effective relationships
  • strong listening and phone skills

Key Requirements

  • Minimum 2 years work experience
  • Minimum 6 months relevant experience
  • Basic knowledge of ICH-GCP
  • Exposure to Microsoft Office Suite

Work Rights

Not specified

Tailored Resume

Cover Letter