Medical Imaging Project Coordinator

Le posteMedical Imaging Project CoordinatorOur 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.ResponsibilitiesReview 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 queriesQuality control of the received imaging data and transmittal formsWork on several projects with different teams (Cincinnati and France)Support of the Project Manager tasks such as for data export request and QCOverall meeting support: organization, agenda, meeting minutes, attendance sheetCoordinate shipmentsInteract with Project Managers, Project Assistant and Imaging TechnologistsReport to the Project ManagerQualificationsBachelor's degree in science or medical related field, clinical trials or related fieldPrior 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 preferredKnowledge of Medical Imaging desirable but not mandatoryUnderstanding 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 skillsGood 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.Voir l'annonce sur le site de l'entreprisePostulerL'entrepriseMedpaceMedpace 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.Fiche complèteSite internet