medpace

Job Summary : 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....

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...

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 Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV 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 the advancement of clinical...

Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV 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 the advancement of clinical...

Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV 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 the advancement of clinical...

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 Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV 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 the advancement of clinical...

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 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...

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...

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 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...

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...

Job Summary : 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...

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...