Clinical Scientist Associate Director (x3)

Amgen Australia Pty Ltd

Lisbon, Portugal
Late-phase clinical trial support
Protocol development and authoring
Clinical data review and analysis
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 is recognized among the top companies in the Best Workplaces™ ranking in Portugal, fostering a culture of innovation, excellence, and purpose.

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 and authoring
  • Clinical data review and analysis
  • Cross-functional team coordination
  • Regulatory document contribution

Nice-to-have

  • Customer-focused mindset
  • Problem-solving approach
  • Results-oriented
  • Ability to handle 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
  • Experience designing, monitoring, and implementing clinical trials

Work Rights

Not specified

Tailored Resume

Cover Letter