LatAm Regulatory Submissions Lead — Clinical Trials Start-Up

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 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 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...

A leading clinical research organization is seeking an experienced Regulatory Submissions Manager for a full-time, office-based role in Mexico City. 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 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...

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 clinical research organization located in Mexico City is seeking a Regulatory Submissions Coordinator to support regulatory submissions and projects in clinical research. The role requires a Bachelor’s degree, 1-3 years of experience in regulatory submissions, and excellent communication skills. You will be mentored and supported as you advance in your...

A leading clinical research organization is seeking a Regulatory Technician for an office-based role in Mexico City. You will manage submissions and data entry within the Clinical Trials Information System (CTIS). Candidates should have advanced English skills and ideally possess 1-2 years of experience in clinical research. The company offers competitive...

Regulatory Technician - Mexico City only – Office based role ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. Regulatory Technician – Mexico...