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Medpace

Global CRO delivering full-service clinical trials

Feasibility Coordinator

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeLondon, UKNo salary listed

About the Job

Requirements

  • A PhD in life sciences or two years of experience in a clinical research organization (clinical trials) is preferred.
  • Some clinical research experience is beneficial.
  • Fluency in English is required.
  • Ability to prioritize multiple projects and tasks within tight timelines.
  • Analytical thinking and attention to detail.
  • Strong written and verbal communication skills.

Responsibilities

  • Coordinate feasibility assessments and deliver high-quality, accurate feasibility data to internal and external teams.
  • Develop preliminary proposal strategy for site and country selection.
  • Conduct outreach to investigative sites to obtain indication- and protocol-specific feedback.
  • Present feasibility results to proposal team members to ensure correct assumptions were applied and strategy aligns with therapeutic and operational experience.
  • Assist project teams with preparation for bid defense meetings.
  • Support departmental process-improvement initiatives and general departmental administrative functions.

Desired Qualifications

  • Working knowledge of feasibility processes and databases is highly desirable.
  • A PhD in life sciences or two years of experience in a clinical research organization (clinical trials) is preferred.

About the Company

Medpace

Global CRO delivering full-service clinical trials

Medpace is a global Contract Research Organization that provides end-to-end clinical development services for pharmaceutical, biotechnology, and medical device companies. It manages Phase I–IV trials from study design and regulatory submissions to monitoring, data management, biostatistics, and final reporting, using a single integrated team. A key differentiator is its ownership of integrated laboratories—global central labs, a bioanalytical lab, and imaging/ECG core labs—ensuring streamlined workflows and consistent data. Its physician-led, scientifically driven approach and single-vendor model aim to reduce sponsor oversight and help bring therapies to market efficiently, with operations in over 40 countries.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Cincinnati, OH
Founded
1992

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