Clinical Scientist Associate Director: Late Development - Obesity

Amgen Inc

Lisbon, Portugal
Hybrid
Doctorate degree in life sciences
3 years of pharmaceutical clinical drug development experience
Experience supporting late-phase drug development
Amgen Inc. is seeking a Clinical Scientist Associate Director for Late Development in the Obesity therapeutic area, located in Lisbon, Portugal. The ideal candidate will support late-phase clinical trials, ensuring high-quality data and compliance with regulatory standards, while thriving in a diverse and innovative workplace culture

Job Summary

  • This role supports late-phase clinical development by contributing to protocol development, study start-up, data review, and analysis activities.
  • The ideal candidate will assist in authoring clinical protocols, study charters, and regulatory documents while ensuring high-quality decision-ready clinical data.
  • Amgen offers a culture of innovation and excellence with flexible work arrangements and generous total rewards plans including healthcare and career benefits.

Matching Summary

Match Score: 85

Amgen Inc. is seeking a Clinical Scientist Associate Director for Late Development in the Obesity therapeutic area, located in Lisbon, Portugal. The ideal candidate will support late-phase clinical trials, ensuring high-quality data and compliance with regulatory standards, while thriving in a diverse and innovative workplace culture.

Skills & Requirements

Must-have

  • Doctorate degree in life sciences
  • 3 years of pharmaceutical clinical drug development experience
  • Experience supporting late-phase drug development
  • Strong communication and presentation skills
  • Knowledge of Good Clinical Practice compliance

Nice-to-have

  • Experience with Spotfire data analysis tools
  • Contributing author for scientific publications
  • Problem-solving results-oriented approach
  • Experience managing consultants and CROs
  • Ability to translate scientific concepts clearly

Key Requirements

  • Doctorate degree plus 3 years experience OR Master's plus 5 years OR Bachelor's plus 7 years
  • Minimum 3 years pharmaceutical clinical drug development experience
  • Working knowledge of study data readout activities
  • Experience contributing to regulatory submission documents

Work Rights

Not specified

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