Medpace - Cincinnati, OH
posted 4 months ago
Medpace is a leading Contract Research Organization (CRO) specializing in providing 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 integral to the success of our projects and will involve working collaboratively with a team to accomplish various tasks and projects. Our therapeutic areas of focus include Microbiology, Oncology/Hematology, Cardiovascular/Metabolic/Renal, Infectious Disease/CNS/Ophthalmology, among others. If you are looking for a fast-paced, collaborative work environment in clinical research and are eager to develop your career further, this is the opportunity for you. As a Project Coordinator, you will engage in clinical trial management on a day-to-day basis, working closely with the project Clinical Trial Manager (CTM) to ensure timely delivery of tasks with a high degree of accuracy. You will be responsible for compiling and maintaining project-specific status reports, interacting with sponsors, study sites, and internal associates, and providing 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, particularly beneficial for those without previous clinical research experience. Our mission is to accelerate the global development of safe and effective medical therapeutics through a scientific and disciplined approach, leveraging local regulatory and therapeutic expertise across all major areas. Join us in making a difference in the lives of patients and families facing various diseases.