Medpace | Study Start Up Manager | Distrito Federal

Job SummaryOur LATAM clinical trial activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager to join our Study Start Up team in Mexico City! This position plays a key role in the clinical trial management process at Medpace. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.ResponsibilitiesEfficiently manage and successfully execute all aspects of global start-up; Perform qualitychecks on submission documents and site essential documents; Prepare and approve informed consent forms; Review pertinent regulations to develop proactive solutions to start-up issues and challenges; Present during bid defenses, general capabilities meetings, and audits.Qualifications***We kindly ask that you submit your CV in English***At least 4 years of regulatory submissions/start-up management experience (leading regulatory/start-up project teams); Knowledge and experience of Clinical Trial Applications within LATAM; Strong oral andwritten communication skills; Team-oriented approach and strong leadership skills; Willing to workin an office-based model; Fluency in English & local language.#J-18808-Ljbffr