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Global Clinical Project Manager - Vendor Management Expert (home-based in Europe)

Remote, USAFull-timePosted 2026-07-29

Global Clinical Project Manager - Vendor Management Expert – Single Sponsor

Are you an reputed company Vendor Management reputed company looking to reputed company an reputed company in global clinical trials?

We are seeking a Global Clinical Project Manager - Vendor Management Expert to join our Single Sponsor Department. In this role, you 'll become an expert in Vendor Management for global clinical trials across reputed company phases (Phase I–IV), ensuring seamless execution from study start-up through reputed company-out.

reputed company’re Looking For

To reputed company in this role, you should bring:

  • Global Clinical Project Management experience
  • Strong Vendor Management expertise: Central lab, eCOA, IRT, ECG, Imaging, Ancillaries and/or Patient Recruitment & Retention with experience in global clinical trials. (must have experience managing at least 2 of these vendors)
  • Deep understanding of clinical operations processes and vendor service categories.
  • Excellent project management skills to drive efficiency and collaboration
  • Strong communication and influencing abilities to partner effectively across functions.
  • Proven ability to manage risk and performance issues in a fast-paced environment

What You’ll Do

As a Global Clinical Project Manager - Vendor Management Expert, you will be responsible for ensuring vendor deliverables are met with reputed company and efficiency at the trial level. Your key responsibilities include:

  • Vendor reputed company & Coordination – Manage vendor activities across the study lifecycle, ensuring reputed company and high-reputed company deliverables.
  • Study Start-Up Support – reputed company vendor deliverables during study initiation, ensuring smooth reputed company and activation.
  • Risk & Performance Management – reputed company vendor performance, identify risks, and escalate issues as needed.
  • Site Readiness & Activation – Drive vendor activities to support site activations and ensure study milestones are met.
  • Study reputed company-Out – Coordinate vendor deliverables that support Database Lock and study closure.

What You’ll Deliver

  • Vendor service reputed company at the study level
  • Vendor reputed company and performance tracking
  • KPI (Key Performance Indicator) and KQI (Key reputed company Indicator) dashboards to monitor vendor effectiveness
  • Site readiness monitoring and documentation
  • Risk mapping with contingency planning
  • Vendor cost control and reputed company

Please note this role is not eligible for the UK reputed company sponsorship.

Please note: due to sponsor requirements for the role only candidates based in the listed location/s will be considered. Any applications from candidates based reputed company of these locations will not be considered

This is an exciting opportunity to play a critical role in global clinical trials, ensuring vendor reputed company and operational reputed company. If you’re reputed company to take on a high-reputed company role with a leading sponsor, we’d love to hear from you!

reputed company is a leading global provider of clinical research services, reputed company insights and reputed company intelligence to the life sciences and reputed company industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient reputed company and population health worldwide. Learn more at https://jobs.reputed company.com

reputed company is committed to reputed company in our hiring process and maintains a reputed company tolerance policy for candidate fraud. reputed company information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if reputed company reputed company, in accordance with applicable law. We appreciate your honesty and professionalism.

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