Associate Centralized Monitoring Lead - Sponsor Dedicated, Poland (hybrid/home-based)

IQVIA UK

Poland
Base: zł102,800.00 - zł190,900.00; bonus/equity: n...
Hybrid
Centralized monitoring activities
Clinical data review
Subject level data review
IQVIA UK is seeking an Associate Centralized Monitoring Lead to manage centralized monitoring activities for clinical studies in Poland, offering a hybrid work environment. The role requires a minimum of 1.5 years of experience in centralized monitoring or risk-based quality management, along with strong communication and organizational skills

Job Summary

  • Lead the execution of Centralized monitoring activities at multiple sites and studies from initiation through to closeout.
  • Review Central Monitoring KRIs, Endpoint Analyses, Quality Tolerance Limits (QTLs), and other analyses on an ad hoc basis or as outlined in the study-specific Central Monitoring Plan (CMP).
  • Provide Mentorship to central monitors and CMA centralized monitoring associates.

Matching Summary

Match Score: 85

IQVIA UK is seeking an Associate Centralized Monitoring Lead to manage centralized monitoring activities for clinical studies in Poland, offering a hybrid work environment. The role requires a minimum of 1.5 years of experience in centralized monitoring or risk-based quality management, along with strong communication and organizational skills.

Salary

Base: zł102,800.00 - zł190,900.00; Bonus/Equity: Not specified; Benefits: Not specified

Skills & Requirements

Must-have

  • Centralized monitoring activities
  • Clinical data review
  • Subject level data review
  • Site performance monitoring
  • ICH/GCP guidelines adherence
  • Develop new analytics proposal

Nice-to-have

  • Cross-cultural collaboration
  • Mentorship of central monitors
  • Subject matter expert
  • Process enhancements

Key Requirements

  • Minimum 1.5 yrs of Central Monitoring or Risk-based quality management Experience
  • Bachelor's Degree Clinical, life sciences, mathematical sciences, or related field, or nursing qualification
  • Minimum of 3 years of relevant work experience
  • Good knowledge of clinical trial conduct
  • Good Clinical system expertise

Work Rights

Not specified

Tailored Resume

Cover Letter