Project CoordinatorMedpace is a leading CRO for Biotech companies and we are currently seeking a full-time, office-based Project Coordinator to join our Clinical Trial Management team. This position will work on a team to accomplish tasks and projects that are instrumental to the company's success. Our therapeutic areas of focus include Microbiology, Oncology/Hematology, Cardiovascular/Metabolic/Renal, Infectious Disease/CNS/Ophthalmology and more.
If you are looking for a fast paced, collaborative work environment in clinical research and want to develop your career even further, then this is the opportunity for you. Medpace provides Project Coordinators a 4-6 week training program that incorporates a virtual and hands on learning experience, especially for those without previous clinical research experience.ResponsibilitiesEngage in clinical trial management on a day to day level;Work closely with the project CTM for timely delivery of tasks consistently with a high degree of accuracy;Compile and maintain project-specific status reports;Interact with the Sponsor, study sites, and internal associates;Provide oversight and quality control of our internal regulatory filing system;Manage study supplies;Create and maintain project timelines; andCoordinate project meetings and produce quality meeting minutes.QualificationsMinimum of a Bachelor's Degree in Life Sciences field;Excellent computer, organizational, and time management skills; andResearch experience preferred.