Clinical Trials Regulatory Specialist.

The Clinical Trials Regulatory Specialist is responsible and accountable for ensuring that inpatient and outpatient research protocols are coordinated through the regulatory process at study start-up and through the life of the study.

Job Description:

  • Full time
  • Knowledge in COFEPRIS Submission Process
  • Knowledge in Submitting to Local IRBs and Ethics Committees
  • Handling documents for the Regulatory Process
  • Preparing Documents for the Regulatory Process
  • Coordinating and assisting with contact database activities, including maintaining updated contact information for organization


  • Academic level of education; Bachelors Degree in areas related to Medical Science, Pharmacology, Biology or similar
  • 2 Years Experience in Clinical Research Industry
  • Adequate command of written and spoken Spanish and English

Our vision is to become leaders in providing clinical research services in Latin America. Cohortias combines academic roots with our experience and a large pool of patients from an extensive network of sites. Join the Cohortias family in Mexico City!.

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