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
Medpace Lea el resumen de esta oportunidad para comprender qué habilidades, incluidas las habilidades interpersonales relevantes y el dominio de paquetes de software, se requieren. Medpace is the leading CRO for Biotech companies and is continuing to add
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
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,
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 is seeking a Clinical Trial Manager for their Madrid office, focusing on CNS/Ophthalmology. ¿Tiene las cualificaciones y habilidades adecuadas para este trabajo? Descúbralo a continuación y pulse en solicitar para ser
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
Study Start Up Manager Join Medpace as a full‑time, office‑based Regulatory Submissions Manager in Mexico City. This role plays a key part in the study start‑up process, building on your experience in clinical trials and regulatory submissions.
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. 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
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
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 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
Study Start Up ManagerJoin Medpace as a full‐time, office‐based Regulatory Submissions Manager in Mexico City. This role plays a key part in the study start‐up process, building on your experience in clinical trials and regulatory submissions. You