Overview:
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.
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 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
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 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.
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