Role OverviewJoin Amgen’s Mission of Serving Patients. 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. The Senior Director, Regulatory Affairs - Global Regulatory Leader – Oncology will lead one or more the Global Regulatory Teams (GRT) in the Regulatory Affairs organization.
What You Will Do
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, that takes into account worldwide regulatory requirements to drive product development, global registration, achievement and maintenance of desired regional labeling, and effective regulatory agency interactions.
Why It Might Be a Fit
The dynamic professional we seek is a leader with these qualifications: Doctorate degree and 5 years of regulatory experience in biotech or science, OR Master’s degree and 9 years of regulatory experience in biotech or science, OR Bachelor’s degree and 11 years regulatory experience in biotech or science.
Requirements
- Doctorate degree and 5 years of regulatory experience in biotech or science
- Master’s degree and 9 years of regulatory experience in biotech or science
- Bachelor’s degree and 11 years regulatory experience in biotech or science
- 5 years experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation or resources
Benefits
- Comprehensive employee benefits package
- Discretionary annual bonus program
- Stock-based long-term incentives
- Award-winning time-off plans
- Flexible work models
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