Join our team at AMGEN Capability Center Portugal as a Clinical Scientist Associate Director to support late-phase clinical development and contribute to protocol development, study start up, data review and monitoring and analysis activities.
Requirements
- Doctorate degree and 3 years of life sciences/healthcare experience OR Master’s degree and 5 years of life sciences/healthcare experience OR Bachelor’s degree and 7 years of life sciences/healthcare experience
- 3 years of pharmaceutical clinical drug development experience
- Demonstrated experience contributing to clinical trial process improvements within a therapeutic area or study team environment
- Industry or academic experience supporting early or late-phase drug development within a relevant therapeutic area or disease indication
- Strong communication and presentation skills in English, with the ability to clearly convey scientific concepts and clinical data to cross-functional teams and leadership audiences, both written and oral
- Experience supporting the design, monitoring, and implementation of clinical trials in compliance with Good Clinical Practice standards and applicable regulatory requirements
- Working knowledge of study data readout activities, including data cleaning, database lock, data extraction, and generation of clinical data outputs
- Experience contributing to regulatory submission documents and supporting clinical regulatory responses for health authority interactions under guidance
- Experience serving as a contributing author on scientific publications or data presentations for internal forums or scientific conferences
- Experience in clinical data analysis such as Spotfire or other data analysis tools
Benefits
- Generous AMGEN Total Rewards Plan comprising healthcare, finance, wealth, and career benefits
- Flexible work arrangements