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Medpace

Global CRO delivering full-service clinical trials

Patient Travel Coordinator

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeDenver, CO, USA

About the Job

Requirements

  • A bachelor's degree is required.
  • At least 3 years of experience in a patient travel and payment service is required.
  • Knowledge and experience of global travel logistics, infrastructure, and cost drivers are required.
  • Knowledge of the pharmaceutical clinical research industry and of how clinical-trial participation affects patients, including the benefits of patient travel support, is required.
  • Prior experience working in a clinical research or healthcare setting is required.
  • Effective time management and the ability to manage multiple projects and timelines are required.
  • Computer literacy and knowledge of Microsoft Office products, including Word, Excel, and PowerPoint, are required.

Responsibilities

  • Serve as the main point of contact for patients and clinic nurses to receive and fulfill travel and payment requests.
  • Work with clients and trial managers to create guidelines and parameters for each new study.
  • Set up new studies by adding them to the portal, setting them up in finance, generating materials from existing templates, and ensuring proper regulatory filing and translations.
  • Onboard clinic nurses at new sites.
  • Liaise with patients or their primary caregivers or family members.
  • Coordinate logistics and translation needs with outside vendors.
  • Plan effectively for future visits and use efficiencies whenever possible.
  • Track spending and prepare monthly usage financial reports.
  • Maintain effective and efficient communication.
  • Provide assistance for patient travel emergencies, including some evening or weekend work.
  • Perform other projects and responsibilities as assigned.

Desired Qualifications

  • Spanish-speaking ability is a bonus but is not essential.

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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