M

Medpace

Global CRO delivering full-service clinical trials

Entry-Level Patient Concierge Coordinator

Clinical Support & Patient AdministrationConfirmed live in the last 24 hours
Full-timeCincinnati, OH, USANo salary listed

About the Job

Requirements

  • A bachelor's degree is required.
  • Knowledge and experience of global travel logistics, infrastructure, and cost drivers.
  • Knowledge of the pharmaceutical clinical research industry and how clinical-trial participation affects patients, including the benefits of this support.
  • Prior experience working within a clinical research or healthcare setting.
  • Effective time-management skills and the ability to manage multiple projects and timelines.
  • Computer literacy and knowledge of Microsoft Office products, including Word, Excel, and PowerPoint.
  • The ability to work some evenings and/or weekends to provide patient travel emergency assistance.

Responsibilities

  • Serve as the main point of contact for patients and clinic nurses to receive and fulfill travel and payment requests.
  • Work with the client and trial manager 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 for new sites.
  • Liaise with patients or their primary caregivers or family members.
  • Coordinate logistics and translation needs with outside vendors.
  • Plan effectively for future visit needs and use efficiencies whenever possible.
  • Track spending and prepare monthly usage financial reports.
  • Maintain effective and efficient communication.
  • Handle other projects and responsibilities as assigned.

Desired Qualifications

  • Experience in a patient-facing role is preferred.
  • Spanish speaking 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

Recently Posted Jobs

Explore more opportunities at Medpace

See more jobs