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
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.
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