Global Feasibility Manager
Job in
Northern, Floyd County, Kentucky, USA
Listed on 2026-09-20
Listing for:
Amgen Inc. (IR)
Full Time
position Listed on 2026-09-20
Job specializations:
-
Research/Development
Clinical Research, Regulatory Compliance Specialist
Job Description & How to Apply Below
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 Feasibility Manager**##
** What you will do
** Let’s do this. Let’s change the world. In this vital role you will will you put your skills, experience and passion to work toward your goals? At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies, reaching over 10 million patients worldwide. Come do your best work alongside other innovative, driven professionals in this meaningful role.
** Live**## What you will doLet’s do this. Let’s change the world. In this vital role you will own the development and execution of the feasibility strategy in partnership with clinical program team, study delivery team, global study management, and cross- functional data teams to deliver a fully-optimized operational action plan. You will lead the successful delivery of the feasibility process (strategy plans, country selection, site identification, timelines, synthesis of feasibility insights) to expedite cycle times for all clinical programs assigned.
* Lead activities pertaining to country and site identification, feasibility and country selection within a clinical study
* Partner with study team members, data analytics team, and country teams to design and conduct global feasibility activities on time with high quality delivery.
* Ensure consistency of feasibility execution across the portfolio/pipeline including bridging gaps between local/central data
* Ensure clear timelines and expectations are aligned and communicated between data providers and study teams to expedite data insight deliverables and confirm the analysis timeline is coordinated with study team decision milestones. This includes initial enrollment timelines, footprint optimization, developing key assumptions, and establishing patient recruitment strategy potential, etc.
* Lead the collection of local internal and external data (e.g. local treatment standard of care, available treatment options approved/reimbursed, local incidence/prevalence of disease, access to targeted patient population, operational barriers) to define an optimal geographic country footprint and proposed sites for participation in a clinical study.
* In partnership with internal partners- synthesize, interpret and integrate data and information to provide clear feasibility recommendations to further embed data-driven decision making, analyze trends, identify root causes, and provide actionable recommendations across study teams and programs to accelerate study execution.
* Facilitate the study baseline commitment & change process (country and study levels).
* Initiate and lead…
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