Centralized Monitoring Asst

IQVIA UK

Multiple Locations, United Kingdom
Onsite
Study level administrative support
System report generation
Study trackers maintenance
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 within project timelines and driving tracking compliance to enable credible data for analysis.
  • Monitors site performance, facilitates early identification of site-level risks/issues, and makes recommendations for timely corrective actions.

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
  • study trackers maintenance
  • 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
  • good data entry skills

Key Requirements

  • Minimum 2 years work experience
  • Minimum 6 months relevant experience
  • Basic knowledge of GCP and regulatory requirements
  • Exposure to Microsoft Applications
  • Effective communication skills
  • Life Sciences or educational equivalent

Work Rights

Not specified

Tailored Resume

Cover Letter