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Clinical Scientist Associate Director, Late Development Oncology

AmgenUnited States🌍 Remote
Full-timeSenior
$170k - $230k
per year
👁️ 5 views📝 0 applicationsPosted 8/18/2026Expires 10/17/2026
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Job Description

Career Category Clinical Development Job Description Join Amgen ’s Mission of Serving Patients At Amgen , if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.

Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year.

Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions.

As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based.

If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. Clinical Scientist Associate Director – Late Development WHAT YOU WILL DO Let’s do this. Let’s change the world.

In this role, the Clinical Scientist Associate Director supports oncology late-phase clinical development by contributing to protocol development, study start-up, data review and monitoring and analysis activities.

Working collaboratively with the study team and clinical leadership, this role focuses on study-level implementation and cross-functional coordination to help ensure high-quality, decision-ready clinical data. Support set up and execution of late phase clinical trials with a focus on data quality.

Assist in authoring clinical protocols, Investigators Brochures and other regulatory documents ensuring consistency and clarity. Provide input into and implementation of data management plan, CRF design, and

Required Skills

clinical developmentprotocol developmentdata reviewmonitoringanalysisdata qualityclinical protocolsInvestigators Brochuresregulatory documentsdata management planCRF design

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