Clinical Scientist Associate Director - Late Development, Oncology
AMGEN
Lisbon, Portugal
Doctorate degree in life sciences
3 years pharmaceutical clinical drug development
Experience with good clinical practice standards
This role supports the set up and execution of late phase clinical trials with a focus on ensuring high-quality data
Job Summary
This role supports the set up and execution of late phase clinical trials with a focus on ensuring high-quality data.
The successful candidate will assist in authoring clinical protocols, Investigators Brochures, and other regulatory documents while collaborating with study teams.
Amgen offers a diverse and inclusive community where colleagues are empowered to bring ideas to the table and take risks.
Matching Summary
This role supports the set up and execution of late phase clinical trials with a focus on ensuring high-quality data.
Skills & Requirements
Must-have
Doctorate degree in life sciences
3 years pharmaceutical clinical drug development
Experience with Good Clinical Practice standards
Protocol development and regulatory document authoring
Data management plan and CRF design oversight
Nice-to-have
Strong communication and presentation skills
Experience with Spotfire or data analysis tools
Contributing author on scientific publications
Ability to manage cross-functional teams
Experience supporting early or late-phase drug development
Key Requirements
Doctorate degree required OR Master's with 5 years experience OR Bachelor's with 7 years experience
Minimum 3 years of pharmaceutical clinical drug development experience preferred
Working knowledge of study data readout activities including database lock