medpace inc

Job SummaryOur Latin American activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical SafetyCoordinator to join our team! This position plays a key role inthe pharmacovigilanceprocess at Medpace.Working in a team to accomplish tasks and projects that are instrumental to the company’s success.If you want an exciting...

Job SummaryOur Latin American activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical SafetyCoordinator to join our team! This position plays a key role inthe in 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...

Medpace in Mexico City seeks a Regulatory Submissions Coordinator to support our Regulatory Submissions team on multiple projects, gaining hands-on experience in study start up and regulatory documentation. You will work alongside experienced coordinators, receive mentoring, and develop regulatory and data management skills in a collaborative, office-based...

Medpace is seeking a full-time, office-based Clinical Safety Coordinator to join our team in Mexico City. This role plays a key part in the pharmacovigilance process and supports global safety activities within a leading CRO.The position involves working in a collaborative team to accomplish tasks instrumental to Medpace's success, with opportunities to...

Join Medpace in our Mexico City office! Medpace is the leading CRO for Biotech companies and is continuing to add established Clinical Trial Managers / Project Managers to join our Clinical Trial Management Group in Mexico City, Mexico. Our therapeutic areas of focus include Oncology, Cardiovascular/Metabolic, Infectious Disease, CNS and more. We offer a...

Medpace in Mexico City seeks a Regulatory Submissions Coordinator to support our Regulatory Submissions team on multiple projects, gaining hands-on experience in study start up and regulatory documentation. You will work alongside experienced coordinators, receive mentoring, and develop regulatory and data management skills in a collaborative, office-based...

Medpace is seeking a full-time, office-based Clinical Safety Coordinator to join our team in Mexico City. This role plays a key part in the pharmacovigilance process and supports global safety activities within a leading CRO.The position involves working in a collaborative team to accomplish tasks instrumental to Medpace's success, with opportunities to...

Job SummaryOur Latin American activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical SafetyCoordinator to join our team! This position plays a key role inthe pharmacovigilanceprocess at Medpace.Working in a team to accomplish tasks and projects that are instrumental to the company’s success.If you want an exciting...

Medpace is seeking a full-time, office-based Clinical Safety Coordinator to join our team in Mexico City. This role plays a key part in the pharmacovigilance process and supports global safety activities within a leading CRO.The position involves working in a collaborative team to accomplish tasks instrumental to Medpace's success, with opportunities to...

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...

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...