Experienced Clinical Trial Manager (Oncology / Cardiovascular / Metabolic / GI)

Company: Medpace
Apply for the Experienced Clinical Trial Manager (Oncology / Cardiovascular / Metabolic / GI)
Location: London
Job Description:

Overview

In this role you drive the day-to-day delivery of clinical trial operations in London within Medpace’s Clinical Trial Management Group. You leverage your therapeutic expertise (Cardiovascular/Endocrine/Metabolic) while ensuring compliance with ICH/GCP and applicable laws. You partner with sponsors and cross-functional teams to manage timelines, risks, vendors, and study deliverables, shaping trial execution at a leading CRO. This is a hands-on role with meaningful impact on trial success and patient outcomes.

Pay / Benefits

  • Flexible work environment
  • Competitive compensation and benefits package
  • Competitive PTO packages
  • Structured career paths with opportunities for professional growth
  • Company-sponsored employee appreciation events
  • Employee health and wellness initiatives

Responsibilities

  • Manage day-to-day operations of trials per contract, ICH/GCP standards and regulations
  • Serve as primary Sponsor contact for operational issues and deliverables
  • Maintain in-depth knowledge of protocol, therapeutic area, and indication
  • Provide cross-functional oversight and ensure project-specific training for team members
  • Review input for study protocol, edit check specs, data analysis plan, and final study report
  • Develop operational project plans and manage risk assessment and execution
  • Oversee study vendors and monitor site quality; supervise CRAs and deliverables

Key requirements

  • Bachelor’s degree in health or life sciences; advanced degree preferred
  • 5+ years of Clinical Trial Management experience; CRO experience preferred
  • Experience in Phases 1-4 (Phases 2-3 preferred)
  • Experience managing overall project timelines; bid defense experience preferred
  • Strong leadership and stakeholder management skills
  • Leadership
  • Cross-functional collaboration
  • Effective communication with sponsors and teams
  • ICH/GCP compliance
  • Protocol review and study design input
  • Data analysis plan and final study report knowledge

Posted: September 14th, 2026