Supports late-phase clinical development by contributing to protocol development, study start-up, data review and monitoring and analysis activities.
Focuses on study-level implementation and cross-functional coordination to ensure high-quality, decision-ready clinical data.
Assists in authoring clinical protocols, Investigators Brochures, and other regulatory documents ensuring consistency and clarity.
Supports review, analysis, and presentation preparation of clinical trial data for internal decision-making, external interactions, and regulatory submission.
Anticipates and actively manages problems across a broad spectrum of cross-functional teams.
Supports appropriate training, recruitment, and development requirements for matrix team resources.

Doctorate degree and 3 years of life sciences/healthcare experience
Master’s degree and 5 years of life sciences/healthcare experience
Bachelor’s degree and 7 years of life sciences/healthcare experience
3 years of pharmaceutical clinical drug development experience (preferred)
Strong communication and presentation skills
Experience supporting the design, monitoring, and implementation of clinical trials
Working knowledge of study data readout activities
Experience contributing to regulatory submission documents and supporting clinical regulatory responses
Experience serving as a contributing author on scientific publications or data presentations (preferred)

Vast opportunities to learn, develop, and move up and across our global organization.
Diverse and inclusive community of belonging, where colleagues are empowered to bring ideas to the table, take risks, and act.
Generous AMGEN Total Rewards Plan comprising healthcare, finance, wealth, and career benefits.
Flexible work arrangements.

Clinical Scientist Director – Late Development, Heart Failure

Key skills