Medical Imaging Project Coordinator

Our imaging services are growing rapidly, and we are currently seeking a full-time, office-based

Project Coordinator to join our team. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.

• Review incoming medical imaging data for clinical trials for initial quality standards.
• Draft and maintain study-related documents (in English)
• Contact with sites (hospitals), all around the word for qualification, follow up and queries
• Quality control of the received imaging data and transmittal forms
• Work on several projects with different teams (Cincinnati and France)
• Support of the Project Manager tasks such as for data export request and QC
• Overall meeting support: organization, agenda, meeting minutes, attendance sheet
• Coordinate shipments
• Interact with Project Managers, Project Assistant and Imaging Technologists
• Report to the Project Manager

• Bachelor's degree in science or medical related field, clinical trials or related field
• Prior experience with clinical trials is a plus (clinical research associate are welcome to apply)
• Prior experience as a Project Coordinator within a CRO or a pharma company is preferred
• Knowledge of Medical Imaging 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 (FDA, EMA, etc.)
• Excellent computer (word-processing, databases, Excel, Windows), organizational, and communication skills
• Good level of English. Should be able to communicate fluently and write documents.

No travel. We kindly request to submit CV in English.

Please apply directly via the Medpace careers portal and not via email.

Medpace is a global Clinical Research Organisation (CRO) partnering with leading pharmaceutical, biotech, and device companies to bring promising new drugs and devices to market. Medpace combines efficient clinical trial management with comprehensive regulatory consulting to provide clients with exceptional support during the drug development process. We manage the full drug and device development process for our clients which includes many components: clinical development plan preparation, project management, regulatory document preparation, safety surveillance, clinical monitoring, data management, statistical analysis, medical writing, quality assurance auditing, and regulatory submissions.

Employing almost 6,000 people across 40+ countries, our people are our biggest asset and embody our values and our approach to serving our clients. They work hard, understand our high expectations, and rise to the challenge. In return, they are rewarded with interesting projects, career advancement, and recognition. Whether you are a recent graduate or seasoned in your field, your contributions can make an impact on our business.