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

IQVIA

Fully remote
Centralized monitoring experience
Subject level data review
Ich gcp regulatory compliance
Lead the execution of Centralized monitoring activities across multiple sites and studies from initiation through closeout

Job Summary

  • Lead the execution of Centralized monitoring activities across multiple sites and studies from initiation through closeout.
  • Ensure subject safety and data integrity while adhering to ICH/GCP guidelines and applicable regulatory requirements.
  • Collaborate with study teams to review structured clinical data output and provide inputs for continuous process improvements.

Matching Summary

Lead the execution of Centralized monitoring activities across multiple sites and studies from initiation through closeout.

Skills & Requirements

Must-have

  • Centralized Monitoring experience
  • Subject Level Data Review
  • ICH GCP regulatory compliance
  • Risk-based quality management
  • Site Visit Report review
  • KRI and QTL analysis

Nice-to-have

  • Mentorship of central monitors
  • Advanced analytics proposal development
  • Strong communication skills
  • Cross-cultural collaboration
  • Process enhancement initiatives

Key Requirements

  • Minimum 3 years relevant work experience
  • Bachelor's Degree in Clinical or Life Sciences
  • 1.5 years Central Monitoring experience
  • Good knowledge of ICH GCP regulations

Work Rights

Not specified

Tailored Resume

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