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Medpace

Global CRO delivering full-service clinical trials

Imaging Project Coordinator

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeLyon, FranceNo salary listed

About the Job

Requirements

  • A BSc, MSc, or PhD in Biomedical Engineering, science, or a medical-related field, clinical trials, or a related field.
  • Prior experience with clinical trials is a plus.
  • Prior experience as a Project Coordinator within a CRO or a pharmaceutical company is preferred.
  • Knowledge of medical imaging is desirable but not mandatory.
  • Understanding of International Conference on Harmonization (ICH) Good Clinical Practice (GCP) guidelines and other regulatory requirements that may impact clinical trials, including FDA and EMA requirements.
  • Computer skills in word processing, databases, Excel, and Windows.
  • A very good level of English, with the ability to communicate fluently and write documents.
  • Organizational and communication skills.

Responsibilities

  • Work on several projects with different teams in the US, APAC, and Europe, interacting with Project Managers, other Project Coordinators, Project Assistants, and Technologists.
  • Perform quality control of incoming medical imaging and cardiovascular data.
  • Communicate daily with sites and hospitals around the world for qualification, data follow-up, and queries.
  • Draft and maintain study-related documents in English.
  • Provide overall meeting support, including organization, agendas, meeting minutes, and attendance sheets.
  • Support the Project Manager's daily activities, such as data export or report requests, database validation and quality control, tracker updates, and Trial Master File-related tasks.
  • Coordinate media shipments.

Desired Qualifications

  • Prior experience with clinical trials is a plus.
  • Prior experience as a Project Coordinator within a CRO or a pharmaceutical company is preferred.
  • Knowledge of medical imaging is desirable but not mandatory.

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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