Medpace - Cincinnati, OH
posted 4 months ago
Medpace is a leading Contract Research Organization (CRO) specializing in providing comprehensive clinical development services to the biotechnology, pharmaceutical, and medical device industries. We are currently seeking a full-time, office-based Project Coordinator to join our Clinical Trial Management team. This position is crucial as it involves working collaboratively within a team to accomplish tasks and projects that are instrumental to the company's success. Our therapeutic area of focus includes Oncology/Hematology, among many others. If you are looking for a fast-paced, collaborative work environment in clinical research and want to develop your career further, then this is the opportunity for you. As a Project Coordinator, you will engage in clinical trial management on a day-to-day level, working closely with the project Clinical Trial Manager (CTM) to ensure timely delivery of tasks with a high degree of accuracy. You will compile and maintain project-specific status reports, interact with the Sponsor, study sites, and internal associates, and provide oversight and quality control of our internal regulatory filing system. Additionally, you will manage study supplies, create and maintain project timelines, and coordinate project meetings while producing quality meeting minutes. Medpace offers a comprehensive 4-6 week training program that incorporates both virtual and hands-on learning experiences, especially beneficial for those without previous clinical research experience.