Medpace - Irving, TX
posted 4 months ago
Medpace is a leading Contract Research Organization (CRO) specializing in clinical trial management for Biotech companies. We are currently seeking a full-time, office-based Project Coordinator to join our Clinical Trial Management team in Dallas, Texas. This role is pivotal in ensuring the success of our clinical trials across various therapeutic areas, including Oncology/Hematology, Cardiovascular/Metabolic/Renal, and Infectious Disease/CNS/Ophthalmology. The Project Coordinator will work collaboratively within a team to manage tasks and projects that are essential to the company's objectives. The position offers a dynamic and fast-paced work environment, ideal for individuals looking to advance their careers in clinical research. Medpace provides a comprehensive 4-6 week training program that combines virtual and hands-on learning experiences, particularly beneficial for those who may not have prior clinical research experience. This training is designed to equip new hires with the necessary skills and knowledge to excel in their roles. As a Project Coordinator, you will engage in daily clinical trial management activities, ensuring that all tasks are completed accurately and on time. You will collaborate closely with the project Clinical Trial Manager (CTM) to deliver recurrent tasks and maintain project-specific status reports. Your role will also involve interacting with sponsors, study sites, and internal associates, providing oversight and quality control of our internal regulatory filing system, managing study supplies, creating and maintaining project timelines, and coordinating project meetings while producing quality meeting minutes.