Global Health Senior Manager
AmgenAbout the role
Career Category
ResearchJob 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.
Global Health Senior Manager
What you will do
Let’s do this. Let’s change the world. In this vital role you will focus on improving the scientific validity and external applicability of clinical research by ensuring that study populations and enrollment strategies are grounded in population-level data and reflect how diseases present and are treated in practice.
- Translate epidemiology and real-world data into actionable study strategies, including burden-aligned enrollment targets, geographic planning, and site selection to better align trials with real-world disease burden.
- Support evaluation of alignment between clinical trial populations and real-world populations across programs, identifying gaps and contributing insights to improve future study design and execution.
- Partner with clinical study teams to influence study design and feasibility decisions, ensuring alignment between trial populations and real-world care delivery.
- Operationalize enrollment strategies that address structural drivers of participation gaps across care settings, moving beyond traditional recruitment approaches.
- Contribute to regulatory deliverables, including Diversity Action Plans (DAPs), by integrating scientific, epidemiologic, and operational insights.
- Support the integration of community-based care settings into clinical research execution, including development of referral pathways and site network strategies that expand access.
- Develop and maintain tools, analytics, and dashboards that enable data-driven decision-making related to enrollment, site performance, and access.
- Track and analyze enrollment performance against population-informed targets, providing recommendations to mitigate risk and improve study outcomes.
- Collaborate cross-functionally (e.g., Clinical Operations, Feasibility, Observational Research, Patient Recruitment) to address operational and structural barriers to participation.
- Provide guidance and training to internal stakeholders on applying population science and data-driven approaches to clinical trial execution.
- Manage external partnerships with research sites, health systems, and community-based organizations to support study execution and access strategies.
- Contribute to testing and refinement of emerging approaches that better connect clinical trials with real-world care delivery.
- Represent Amgen externally through participation in industry forums, working groups, and conferences.
What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The qualified professional we seek is a innovative thinker and cross-functional collaborator with these qualifications.
Basic Qualifications:
Doctorate degree and 2 years of clinical research or public health experience
OR
Master’s degree and 4 years of clinical research or public health experience
OR
Bachelor’s degree and 6 years of clinical research or public health experience
OR
Associate’s degree and 10 years of clinical research or public health experience
OR
High school diploma / GED and 12 years of clinical research or public health experience
Preferred Qualifications:
- Experience translating epidemiologic or real-world data into clinical or operational strategy
- Strong understanding of clinical trial design, feasibility, and execution
- Ability to influence cross-functional stakeholders in complex organizational environments
- Familiarity with regulatory expectations related to clinical trial enrollment planning (e.g.,
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