Medical Imaging Project Coordinator

Join or sign in to find your next job Join to apply for the Medical Imaging Project Coordinator role at Medpace 3 days ago Be among the first 25 applicants 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 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. Medpace 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, we employ more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks Flexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Company-sponsored employee appreciation events Employee health and wellness initiatives Awards Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What To Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. Seniority level Not Applicable Employment type Full-time Job function Other Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Medpace by 2x #J-18808-Ljbffr