Overview Consulte la descripción del puesto a continuación. Si confía en que tiene las habilidades y la experiencia adecuadas, envíe su solicitud hoy mismo. Our CRA Team is currently seeking a full-time home-based CRA located in
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
Job SummaryJoin Medpace at our Mexico City office! Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, Site Contract Manager to join our LatAm Site Contracts team within the Clinical Operations department.
Job SummaryJoin 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
Job Summary: The Clinical Research Associate at Medpace is offering the unique opportunity to have an exciting career in the research of drug and medical device development. For those with medical and/or health/life science interest and background
Join Medpace at our Mexico City office! 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
Medpace, Inc. is seeking a full-time Site Contract Manager in Mexico City to enhance its LatAm Site Contracts team. You will lead contract teams as the primary contact between the sponsor and study teams, manage contract negotiations,
Job Summary: Join Medpace in our Mexico City office! 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
Job Summary: Join Medpace in our Mexico City office! Medpace is the leading CRO for Biotech companies and is continuing to add established Project Managers to join our Clinical Trial Management Group in Mexico City, Mexico . Our
Job Summary: Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Study Start-Up Manager (Regulatory Submissions Manager) to support our growing Study Start-Up/Regulatory Submissions team at Medpace! This position plays a
Job Summary: The Clinical Research Associate at Medpace is offering the unique opportunity to have an exciting career in the research of drug and medical device development. For those with medical and/or health/life science interest and background
Medpace, Inc. is seeking a Regulatory Submissions Coordinator in Mexico City to provide support for regulatory submissions and gain hands-on experience in clinical research. The role involves assisting with document collection, supporting submission managers, and ensuring compliance
Job Summary Our 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
Job Summary Join Medpace at our Mexico City office! Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, Site Contract Manager to join our LatAm Site Contracts team within the Clinical Operations
Job Summary: 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 Meixco City! This position plays a key
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
Medpace, Inc. in Mexico City is seeking a full-time Clinical Safety Coordinator. In this role, you will oversee the submission of safety reports and interact with various departments to ensure compliance with safety regulations. A Bachelors degree
A clinical research organization in Mexico City is seeking a Regulatory Submissions Coordinator to support Regulatory Submissions and gain vital experience in study start-up. Responsibilities include providing support activities, ensuring compliance, and conducting document quality control.
A leading clinical research organization in Mexico City is seeking an experienced Regulatory Submissions Manager for a full-time, office-based role. This position is crucial for the study start-up process, requiring a bachelors degree in life sciences
Job Summary: Our Latin American activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Safety Coordinator to join our team! This position plays a key role in the pharmacovigilance process at Medpace. Working