Empleos de Medpace en México

We are seeking a full-time Clinical Safety Coordinator to join our team. · ...

Experienced Study Start Up Specialist · Medpace is a full-service clinical contract research organization (CRO) with operations in over 40 countries. We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. · Responsi ...

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 ...

Regulatory Submissions Coordinator · About the Role: · At Medpace, we are seeking a highly organized and detail-oriented Regulatory Submissions Coordinator to support our team in ensuring compliance with regulatory requirements. This is an excellent opportunity to gain vital expe ...

Join Medpace, a full-service clinical contract research organization (CRO), in our rapidly expanding LATAM operations. We seek a Supply Chain Specialist - CRO Logistics to work in Mexico City, managing Import & Export activities and vendors for clinical trial projects. · Responsi ...

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 y ...

We are seeking a full-time Site Contract Manager to join our LatAm Site Contracts team within the Clinical Operations department. · We invite you to be part of something that is impacting millions of people around the globe while enjoying a competitive total compensation and bene ...

We are seeking a full-time Clinical Safety Coordinator to join our team This position plays a key role in the pharmacovigilance process at Medpace. · Oversight of submission of safety reports in the appropriate format to Competent Authorities/Ethics Committees in compliance with ...

Study Start Up Manager · This key position plays a pivotal part in the study start-up process. · Efficiently manage global start-up from submission documents through informed consent forms. · ...

Job Title: Regulatory Start-Up Lead – LATAM Trials · A leading clinical research organization requires an experienced Regulatory Submissions Manager to support study start-up processes. · Bachelor’s degree in life sciences. · No less than four years of relevant professional exper ...

Experienced Clinical Safety Coordinator · We are seeking a full-time, office-based Clinical SafetyCoordinator to join our team in Mexico City. This position plays a key role in the pharmacovigilance process at Medpace. · Oversight of submission of safety reports in compliance wit ...

Supply Chain Specialist · A key role within Medpace’s LATAM CRO logistics team is available for a full-time Supply Chain Specialist. The successful candidate will be responsible for the import and export of goods related to clinical trials, ensuring compliance with regulations th ...

Global Clinical Safety Coordinator · This is a full-time role at Medpace, where we oversee the submission of safety reports and ensure compliance with regulatory guidelines. The ideal candidate holds a Bachelor's degree in Life Science and has at least 3 years of experience in dr ...

We are currently seeking a full-time 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. · ...

We are seeking a full-time office based Supply Chain Specialist to join our team in Mexico City. This position will work on a team to accomplish tasks and projects that are instrumental to the company's success. · ...

We are seeking a full-time Regulatory Submissions Manager to join our Study Start Up team in Mexico City. · ...