Study Start-Up Project Manager - Rare DiseaseJob LocationsUnited States-OH-Cincinnati | United States-TX-Irving (Dallas) | United States-CO-DenverCategorySite Activation & MaintenanceJob SummaryDo you enjoy working in a fast-paced environment where you are empowered to make strategic decisions and contribute to a growing and profitable company? Are you tired of voicing ideas that go unheard? Join us at Medpace! Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, Senior Global Study Start-Up Lead to join our Clinical Operations team. This position plays a key role in the clinical trial management process at Medpace.Incentives can include: Competitive bonus program, sign-on/relocation bonus, and equity awards.Location: Position can be office based in Cincinnati, Dallas or Denver.#remote.ResponsibilitiesEfficiently manage successful execution of global start-up, maintenance, and close-out;Effectively lead others in a matrix environment;Perform quality checks on submission documents and site essential documents;Prepare and approve informed consent forms;Serve as a Sponsor point of contact for start-up and regulatory submissions items;Review pertinent regulations to develop proactive solutions to start-up challenges;Prepare new business proposals and present during bid defenses, general capabilities meetings, and audits; andContribute to the growth and development of departmental staff, processes, and systems.QualificationsBachelor's degree required, advanced degree in Life Sciences preferred5+ years of experience in clinical research, preferably in a Senior/Lead role at a CRO in Study Start-UpExperience in the area of rare diseases for clinical trials, e.g., Duchenne Muscular Dystrophy, Epilepsy, Cystic Fibrosis, Amyotrophic Lateral Sclerosis (Lou Gehrig's), etc.Project management experience and demonstrated role in developing othersStrong oral and written communication skills requiredTravel: MinimalMedpace OverviewMedpace 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 PerksCincinnati Campus OverviewHybrid work-from-home options (dependent upon position and level)Competitive PTO packages, starting at 20+ daysFlexible work hoursDiscounted tuition for UC online programsCompany-sponsored employee appreciation eventsEmployee health and wellness initiativesCommunity involvement with local nonprofit organizationsCompetitive compensation and benefits packageStructured career paths with opportunities for professional growthPartnership and discount with onsite childcareDiscounts on local sports games, local fitness gyms and attractionsOfficial Sponsor of FC CincinnatiModern, ecofriendly c