Clinical Scientist Associate Director: Late Development - Obesity
AMGEN
Lisbon, Portugal
Not specified (assumed to be hybrid based on company culture and location).
Doctorate degree in life sciences
3 years pharmaceutical clinical drug development
Experience with late-phase clinical trials
Amgen is seeking a Clinical Scientist Associate Director for Late Development in the Obesity therapeutic area, based in Lisbon, Portugal. The ideal candidate should have a strong background in life sciences and experience in clinical trial management, with a focus on data quality and regulatory compliance
Job Summary
This role supports late-phase clinical development by contributing to protocol development, study start-up, and data review activities within the Obesity therapeutic area.
The ideal candidate will collaborate with clinical leadership to ensure high-quality, decision-ready clinical data through effective cross-functional coordination.
Amgen offers a culture of innovation and excellence with generous total rewards including healthcare, finance, wealth, and career benefits.
Matching Summary
Match Score: 85
Amgen is seeking a Clinical Scientist Associate Director for Late Development in the Obesity therapeutic area, based in Lisbon, Portugal. The ideal candidate should have a strong background in life sciences and experience in clinical trial management, with a focus on data quality and regulatory compliance.
Skills & Requirements
Must-have
Doctorate degree in life sciences
3 years pharmaceutical clinical drug development
Experience with late-phase clinical trials
Knowledge of Good Clinical Practice (GCP)
Ability to author clinical protocols
Nice-to-have
Strong communication and presentation skills
Experience with Spotfire data analysis tools
Contributing author for scientific publications
Problem-solving and results-oriented approach
Experience managing consultants and CROs
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