Empleos de Medpace en México

Join Medpace at our Mexico City office as a Regulatory Submissions Coordinator. You will support many projects and gain vital experience in study start up. · ...

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 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. · ...

Overview · This Clinical Safety Coordinator role plays a key part in Medpace's pharmacovigilance process working on submissions of safety reports worldwide alongside other teams. · Duties & Responsibilities: · Maintain accurate submission records with timely compliance; · Interac ...

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

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 ...

We are currently seeking a full-time Clinical Safety Coordinator to join our team This position plays a key role in the pharmacovigilance process at Medpace. · ...

Study Start Up Manager · Role Overview: Medpace is seeking a Study Start-up Manager with expertise in clinical trials and regulatory submissions in Mexico City. This role plays a key part in the study start-up process. · ...

Supply Chain Specialist · A leading clinical research organization in Mexico City seeks an experienced Supply Chain Specialist. Key responsibilities include: · Coordinating import/export activities for clinical trials. · The ideal candidate should possess: · A Bachelor's degree. ...

The Regulatory Submissions Manager will be responsible for leading regulatory start-up processes, ensuring compliance with regulations and laws. · Responsibilities: · Lead regulatory submissions · Evaluate study protocols against country-specific requirements · ...

Job Description · A global clinical research organization is seeking a full-time Clinical Safety Coordinator. The role is crucial for overseeing safety report submissions requiring at least 3 years of drug safety experience along with a Bachelor's degree in Life Sciences. · Frequ ...

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 Site Contract Manager to join our LatAm Site Contracts team within the Clinical Operations department.This position will report to the LatAm Senior Contract Manager and will play a key role in the study start-up and clinical trial management processes a ...

Join Medpace at our Mexico City office as a Regulatory Submissions Coordinator. The role involves working within Regulatory Submissions, supporting projects and gaining experience in study start up. · ...

Job Summary · We are seeking a full-time Supply Chain Specialist - CRO Logistics. You will manage import/export activities for clinical trials in Mexico. · Communicate with exporters, brokers, customs agents, couriers. · Support regulatory submission team to ensure compliant stud ...

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

About This Role · Join Medpace at our Mexico City office as a Study Start Up Specialist. · Support Regulatory Submissions Coordinators to gain hands-on experience in clinical research. · ...

Regulatory Submissions Coordinator Job Description · This role is designed to support regulatory submissions while gaining valuable experience in study start-up. · Provide support activities as needed · Evaluate compliance with established regulations · Conduct quality control ch ...