Job Information
Medpace, Inc. Supervisor in Cincinnati, Ohio
Clinical Trial Project Manager - Microbiology Specialist (Sign-On Bonus Eligible) Job Locations United States-OH-Cincinnati | United States Category Clinical Trial Management Job Summary Medpace is the leading CRO for Biotech companies and is continuing to add established Clinical Trial Managers and Project Managers with a focus on Microbiology to join our Clinical Trial Management Group. We are involved in designing and conducting a range of global Phase I-IV clinical trials in antivirals, antibacterials, antifungals and vaccines, spanning both adults and pediatrics. We have just expanded our campus in Cincinnati and have offices in Dallas and Denver and provide remote flexibility with relevant experience. We offer a very competitive salary/bonus program which have become very lucrative for our associates. Responsibilities Manage and provide accountability for day-to-day microbiological operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations; Serve as primary Sponsor contact for microbiological operational project-specific issues and study deliverables; Maintain in depth knowledge of protocol, therapeutic area, and indication; Coordinates with all functional areas to ensure microbiological and clinical data are being captured and cleaned appropriately; Develops general and project-specific training related to microbiological operations; Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable; Performs ongoing review of study data to monitor study populations (e.g. microbiological-MITT) and identify trends or issues in the study; Manage risk assessment and execution; and Supports study team in assessing and supporting site's clinical and microbiological laboratories as well as serving as liaison to central laboratories. Qualifications Bachelor's Degree, PhD or Masters in health related field preferred, including, Nursing, Medical Technology, Microbiology, Immunology, Biology, etc.; Experience in medical technology preferred; Clinical and/or laboratory experience in microbiology or clinical experience in Infectious Disease; Previous working experience within the clinical research, project management experience preferred; 5+ years as a project/clinical trial manager within a CRO; required for home-based; and Strong leadership skills. 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, employing 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. Cincinnati Perks Cincinnati Campus Overview Hybrid work-from-home options (dependent upon position and level) Competitive PTO packages, starting at 20+ days Flexible work hours Discounted tuition for UC online programs Company-sponsored employee appreciation ev