Associate Centralized Monitoring Lead

My Medical Sales Jobs

Fully remote
Centralized monitoring plan
Clinical risk identification
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 and in accordance with our SOPs, policies and practices

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 and in accordance with our SOPs, policies and practices.
  • 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.
  • Support in efficient and effective review of Site Visit Reports and assure consistent standards of implementation for quality to meet or exceed quality standards.

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 and in accordance with our SOPs, policies and practices.

Skills & Requirements

Must-have

  • Centralized monitoring plan
  • Clinical risk identification
  • Subject safety and data integrity
  • ICH/GCP guidelines compliance
  • Site visit report review
  • Clinical data review

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 or centralized monitor role preferred
  • Good knowledge of clinical trial conduct and regulatory requirements (ICH GCP)

Work Rights

Not specified

Tailored Resume

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