Regulatory Start-Up Specialist — Study Submissions

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. Requirements include a Bachelor's degree in Life Sciences, 1-3 years...

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 a productive member of the team, and will be mentored and supported as you develop your skills. Working directly with...

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 a productive member of the team, and will be mentored and supported as you develop your skills. Working directly with...

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. You will use your expertise to develop and grow your career while supporting our LATAM clinical trial...

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. You will use your expertise to develop and grow your career while supporting our LATAM clinical trial...

A leading clinical research organization in Mexico City is seeking a Regulatory Submissions Manager to oversee the start-up process for clinical trials. Candidates should have at least 4 years of relevant experience with strong communication and leadership skills. The role is office-based with a focus on managing global start-up activities and ensuring the...

A global provider of clinical research services is seeking a Regulatory and Start Up Specialist in Mexico City. This role involves end-to-end site management, acting as a point of contact for investigative sites, and ensuring compliance with regulatory requirements. The ideal candidate will have a Bachelor’s degree in Life Sciences or related fields and at...

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 bachelor's degree in life sciences and at least 4 years of relevant experience. Candidates should be fluent in English and the local language...

A leading clinical research organization in Mexico City is seeking a Regulatory Submissions Manager to oversee the start-up process for clinical trials. This office-based role requires at least 4 years of relevant experience, strong communication, and leadership skills. Ideal candidates will manage global start-up activities and ensure the quality of...

FSP - Regulatory and Start Up Specialist page is loaded## FSP - Regulatory and Start Up Specialistlocations: Mexico City, Mexicotime type: Full timeposted on: Posted Todayjob requisition id: R1520119**Job Overview**This position will be responsible for participating in end-to-end site management from feasibility to site closure, serving as a **point...