Clinical Scientist Associate Director: Late Development - T2d (x3)

AMGEN

Lisbon, Portugal
Not specified (assumed to be hybrid based on industry norms).
Doctorate degree in life sciences
3 years pharmaceutical clinical development experience
Experience with good clinical practice compliance
AMGEN is seeking a Clinical Scientist Associate Director for Late Development in Lisbon, Portugal, to support late-phase clinical trials and ensure high-quality clinical data. The ideal candidate should possess significant experience in clinical drug development and strong communication skills, contributing to protocol development, data review, and cross-functional collaboration

Job Summary

  • This role supports late-phase clinical development by contributing to protocol development, study start-up, and data review activities.
  • The successful candidate will assist in managing collaborators, consultants, and CROs while ensuring high-quality decision-ready clinical data.
  • Amgen offers a culture of innovation and excellence with flexible work arrangements and opportunities for global career growth.

Matching Summary

Match Score: 85

AMGEN is seeking a Clinical Scientist Associate Director for Late Development in Lisbon, Portugal, to support late-phase clinical trials and ensure high-quality clinical data. The ideal candidate should possess significant experience in clinical drug development and strong communication skills, contributing to protocol development, data review, and cross-functional collaboration.

Skills & Requirements

Must-have

  • Doctorate degree in life sciences
  • 3 years pharmaceutical clinical development experience
  • Experience with Good Clinical Practice compliance

Nice-to-have

  • Strong communication and presentation skills
  • Experience with Spotfire data analysis tools
  • Contributing author for scientific publications

Key Requirements

  • Doctorate degree plus 3 years experience OR Master's plus 5 years OR Bachelor's plus 7 years
  • Minimum 3 years of pharmaceutical clinical drug development experience
  • Working knowledge of study data readout activities including database lock and extraction

Work Rights

Not specified

Tailored Resume

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