Clinical Scientist Associate Director

Amgen UK

Lisbon, Portugal
Late-phase clinical trial support
Protocol development
Data quality focus
Supports late-phase clinical development by contributing to protocol development, study start-up, data review and monitoring, and analysis activities

Job Summary

  • Supports late-phase clinical development by contributing to protocol development, study start-up, data review and monitoring, and analysis activities.
  • This role focuses on study-level implementation and cross-functional coordination to help ensure high-quality, decision-ready clinical data.
  • Amgen UK is consistently recognized among the top companies in the Best Workplaces™ ranking by Great Place to Work® in Portugal.

Matching Summary

Supports late-phase clinical development by contributing to protocol development, study start-up, data review and monitoring, and analysis activities.

Skills & Requirements

Must-have

  • Late-phase clinical trial support
  • Protocol development
  • Data quality focus
  • Cross-functional coordination
  • Medical monitoring

Nice-to-have

  • Customer-focused mindset
  • Problem-solving approach
  • Results-oriented
  • Handling multiple tasks

Key Requirements

  • Doctorate degree and 3 years of life sciences/healthcare experience
  • Master’s degree and 5 years of life sciences/healthcare experience
  • Bachelor’s degree and 7 years of life sciences/healthcare experience
  • 3 years of pharmaceutical clinical drug development experience

Work Rights

Not specified

Tailored Resume

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