Medical Imaging Project Coordinator

Medpace; Lyon; Sur place; EUR 40 000 - 60 000; Plein temps

Résumé du poste

Join a dynamic and rapidly growing imaging services team as a Project Coordinator. This full-time, office-based position offers the chance to leverage your expertise while further developing your career in a supportive environment. You will be responsible for reviewing medical imaging data, maintaining study documents, and coordinating with international sites. If you thrive in a collaborative atmosphere and are eager to contribute to impactful clinical trials, this opportunity is perfect for you. Embrace the chance to make a difference in the healthcare landscape while advancing your professional journey.

Qualifications

• Bachelor's degree in a relevant field is required.
• Prior experience with clinical trials is a plus.

Responsabilités

• Review medical imaging data for quality standards.
• Draft study-related documents and coordinate shipments.

Connaissances

Organizational Skills

Communication Skills

Computer Skills

Knowledge of Clinical Trials

Fluent English

Formation

Bachelor's degree in science or medical related field

Outils

Microsoft Word

Microsoft Excel

Databases

Description du poste

Job Summary

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.

Responsibilities

• 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 world 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

Qualifications

• Bachelor's degree in science or medical related field, clinical trials or related field
• Prior experience with clinical trials is a plus (clinical research associates 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.