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Regulatory Affairs Senior Director - Global Regulatory Leader - Oncology

AmgenUnited States🌍 Remote
Full-time15+
$215k - $291k
per year
👁️ 0 views📝 0 applicationsPosted 8/10/2026Expires 10/9/2026
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Job Description

Career Category Regulatory 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. Senior Director, Regulatory Affairs - Global Regulatory Leader – Oncology What you will do Let’s do this.

Let’s change the world. Amgen is seeking a Senior Director, Regulatory Affairs supporting products in the Oncology Therapeutic Area. Global Regulatory Affairs (GRA) provides global regulatory leadership, expertise, and execution for the development, registration, and life cycle management of all Amgen molecules.

In this vital, product-facing role you will lead one or more the Global Regulatory Teams (GRT) in the Regulatory Affairs organization.

The purpose of the Global Regulatory Affairs Senior Director is: To lead GRTs within Amgen ’s GRAAS organization To independently develop a comprehensive regulatory strategy for one or more high complexity programs, typically in late-stage development and/or with multiple indications, tha

Required Skills

Regulatory AffairsOncologyGlobal Regulatory StrategyLate-Stage DevelopmentRegulatory SubmissionsLife Cycle ManagementTherapeutic Area ExpertiseRegulatory LeadershipRegulatory ComplianceRegulatory Approvals

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