medpace

Join Medpace at our Mexico City offfice! As a Regulatory Submissions Coordinator you will have the opportunity to work within Regulatory Submissions, supporting our many projects and gaining vital experience in study start up! You will be a productive member of the team, and will be mentored and supported as you develop your skills. Working directly with...

Medpace Mexico City is seeking a full-time, office-based Clinical Research Project Coordinator to join the Clinical Trial Management team.You will work on a team to accomplish tasks and projects that are instrumental to the company's success.Responsibilities include managing day-to-day clinical trial activities, coordinating with the CTM, preparing status...

Our 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 study start up process at Medpace. If you want an exciting career where you use your previous expertise and can develop and grow...

Job Summary :Join Medpace in Mexico City!We are currently seeking a full-time, office-based Clinical Research 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.If you want an exciting career where you use your previous expertise and...

Medpace is seeking seasoned Clinical Trial Managers / Project Managers to join our Mexico City office, leading day-to-day operations for trials across Phases 1–4.You will coordinate cross-functional teams, ensure adherence to ICH/GCP, and serve as primary sponsor contact for study deliverables.You will oversee site quality, risk management, and vendor...