Latam Hub Head, Global Site & Study Operations, Associate Director

Amgen UK

Base: not specified; bonus/equity: discretionary a...
Fully remote
Clinical research experience in biopharmaceuticals
Direct people management and leadership experience
End-to-end study and site execution oversight
The role provides strategic and operational leadership for all study and site execution within the assigned LATAM hub geography to ensure delivery of the clinical portfolio

Job Summary

  • The role provides strategic and operational leadership for all study and site execution within the assigned LATAM hub geography to ensure delivery of the clinical portfolio.
  • Candidates must have significant experience managing clinical operations, overseeing vendors such as CROs and central labs, and ensuring regulatory compliance with ICH-GCP standards.
  • Amgen offers a comprehensive Total Rewards Plan including health benefits, retirement savings, discretionary bonuses, stock incentives, and flexible work models.

Matching Summary

The role provides strategic and operational leadership for all study and site execution within the assigned LATAM hub geography to ensure delivery of the clinical portfolio.

Salary

Base: Not specified; Bonus/Equity: Discretionary annual bonus program and stock-based long-term incentives; Benefits: Comprehensive employee benefits package including retirement plan, medical/dental/vision coverage, and flexible work models

Skills & Requirements

Must-have

  • Clinical research experience in biopharmaceuticals
  • Direct people management and leadership experience
  • End-to-end study and site execution oversight
  • Vendor and CRO management capabilities
  • Regulatory compliance and ICH-GCP knowledge

Nice-to-have

  • Strong understanding of local regulatory requirements
  • Experience with global portfolio priorities
  • Advanced English proficiency
  • Innovation in site engagement strategies
  • Collaborative and science-based culture fit

Key Requirements

  • Doctorate degree plus 3 years clinical experience OR Master's plus 7 years OR Bachelor's plus 9 years
  • At least 3 years of direct people management or leadership experience
  • 6 years of biopharmaceutical clinical research experience
  • Experience at or oversight of clinical research vendors (CROs, central labs)
  • Advanced English proficiency required

Work Rights

Not specified

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