Senior Associate Regulatory Affairs - Clinical Studies (cdmx)

Amgen UK

Mexico City, Mexico
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Clinical study authorizations
Regulatory documentation
Health authority collaboration
** Amgen UK is seeking a Senior Associate in Regulatory Affairs for Clinical Studies in Mexico City. The role involves providing regulatory leadership for clinical studies, ensuring compliance with local regulations, and collaborating with cross-functional teams to support timely approvals. **

Job Summary

  • The Local Senior Associate Regulatory Affairs provides high-level regulatory leadership for Amgen-sponsored clinical studies in Mexico.
  • The role independently drives local regulatory strategy, decision-making, and execution to ensure timely, compliant clinical trial authorizations and lifecycle management.
  • Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards.

Matching Summary

Match Score: 75

** Amgen UK is seeking a Senior Associate in Regulatory Affairs for Clinical Studies in Mexico City. The role involves providing regulatory leadership for clinical studies, ensuring compliance with local regulations, and collaborating with cross-functional teams to support timely approvals. **

Skills & Requirements

Must-have

  • clinical study authorizations
  • regulatory documentation
  • health authority collaboration
  • GCP compliance
  • regulatory risk assessment

Nice-to-have

  • collaborative culture
  • science-based approach
  • patient-focused mission

Key Requirements

  • Master’s degree in health sciences or related field and experience in Clinical Regulatory Affairs in Mexico
  • Bachelor’s degree in health sciences or related field and 2 years of experience in Clinical Regulatory Affairs in Mexico
  • Associate’s degree in health sciences or related field and 6 years of experience in Clinical Regulatory Affairs in Mexico
  • Proficiency in English, both in oral and written communication

Work Rights

Not specified

Tailored Resume

Cover Letter