Associate Centralized Monitor - Poland

IQVIA UK

Warsaw, Poland
Base: zł80,500.00 - zł149,500.00; bonus/equity: no...
Onsite
Centralized monitoring activities
Subject level data review
Clinical systems proficiency
Provide study level administrative support to the clinical study management team, including running system reports and preparing status updates

Job Summary

  • Provide study level administrative support to the clinical study management team, including running system reports and preparing status updates.
  • Perform centralized monitoring activities on assigned sites, evaluating quality and integrity as per protocol, SOPs, and regulations.
  • Facilitate early identification of site-level risks and monitor site performance, making recommendations for corrective actions.

Matching Summary

Provide study level administrative support to the clinical study management team, including running system reports and preparing status updates.

Salary

Base: zł80,500.00 - zł149,500.00; Bonus/Equity: Not specified; Benefits: Not specified

Skills & Requirements

Must-have

  • Centralized monitoring activities
  • Subject level data review
  • Clinical systems proficiency
  • ICH-GCP and regulatory knowledge
  • Site communication and follow-up

Nice-to-have

  • Results and detail-oriented approach
  • Problem-solving skills
  • Strong telecommunication skills
  • Attention to detail and accuracy

Key Requirements

  • 2 to 5 years of work experience
  • Minimum 1 year relevant experience
  • Graduate/Post Graduate in Life Sciences
  • Proficient in Clinical Systems (EDC, IXRS, CTMS)
  • Good command of English language
  • Good command of Czech and Slovak language

Work Rights

Not specified

Tailored Resume

Cover Letter