Study Management Specialist

3 days ago


London, Greater London, United Kingdom Medpace Full time

Role Summary

This Study Management Specialist will manage and provide accountability for day-to-day operations of projects, serving as the primary Sponsor contact for operational project-specific issues and study deliverables.

Key Responsibilities

  • Manage and provide accountability for day-to-day operations of projects
  • Serve as primary Sponsor contact for operational project-specific issues and study deliverables
  • Maintain in-depth knowledge of protocols, therapeutic areas, and indications

What You'll Need

  • Bachelor's degree in a health or life science-related field
  • Advanced degree in a health or life science-related field preferred
  • Experience in Phases 1-4, with a preference for Phases 2-3
  • Minimum 5 years of Clinical Trial Management experience, with CRO experience preferred

Why Choose Medpace

Medpace is a leading CRO that provides Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. As a member of our team, you will have the opportunity to work on high-profile projects and contribute to the development of safe and effective medical therapeutics.



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