Associate Centralized Monitoring Lead

IQVIA

Multiple Locations
Fully remote
Centralized monitoring plan
Clinical risk management
Subject safety and data integrity
Provides support to CMS leads on activities related to the CMS team, in partnership with project and clinical lead, and in collaboration with other functional teams, to achieve the delivery of the project’s overall objectives to the sponsor’s satisfaction per contract while optimizing speed, quality and cost of delivery

Job Summary

  • Provides support to CMS leads on activities related to the CMS team, in partnership with project and clinical lead, and in collaboration with other functional teams, to achieve the delivery of the project’s overall objectives to the sponsor’s satisfaction per contract while optimizing speed, quality and cost of delivery.
  • Associate Centralized Monitoring Lead has particular focus on supporting the centralized team functionally reporting to leads towards solutions to clinical risks identified and working towards successful implementation of those strategies to address the issues.
  • Ensure subject safety, data integrity, escalation of issues and timely and responsive feedback in compliance with IQVIA SOP, ICH/ GCP guidelines, protocol requirements and regulatory compliance.

Matching Summary

Provides support to CMS leads on activities related to the CMS team, in partnership with project and clinical lead, and in collaboration with other functional teams, to achieve the delivery of the project’s overall objectives to the sponsor’s satisfaction per contract while optimizing speed, quality and cost of delivery.

Skills & Requirements

Must-have

  • Centralized monitoring plan
  • Clinical risk management
  • Subject safety and data integrity
  • ICH/GCP guidelines compliance
  • Study metrics trending
  • Quality reviews of analytical output

Nice-to-have

  • Cross-functional team collaboration
  • Continuous process improvement
  • Cultural awareness and adaptability
  • Mentoring and coaching junior staff

Key Requirements

  • Bachelor's Degree in Clinical, life sciences, mathematical sciences, or related field, or nursing qualification
  • Minimum 4 years of relevant work experience
  • At least 2 years of experience in clinical research field or centralized monitor role preferred
  • Good knowledge of clinical trial conduct and regulatory requirements
  • Good Clinical system expertise
  • Ability to work on multiple projects and manage competing priorities

Work Rights

Not specified

Tailored Resume

Cover Letter