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Salary
$71k – $160k per year (Estimated)
Location
Remote/Hybrid (London, Cambridge, United Kingdom)
Seniority
Staff
Employment
Full-Time
Overview
Company
Impact
Profile match
Amgen is an American biotechnology company founded in Thousand Oaks in 1980 that became one of the first firms to turn recombinant protein research into large commercial medicines. Its history rests on Epogen and Neupogen, and its current portfolio spans bone health with Prolia and Evenity, inflammation with Otezla and Tezspire, cardiovascular disease with Repatha, oncology including the bispecific antibody Blincyto, and a biosimilars business built on its own manufacturing capacity. The company is listed on Nasdaq, is a component of the Dow Jones Industrial Average, and expanded further into rare disease through its acquisition of Horizon Therapeutics.

Career Category

Clinical

Job Description

If you feel like you’re part of something bigger, it’s because you are. 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. We are global collaborators who achieve together-researching, manufacturing and delivering ever-better products that reach over 10 million patients worldwide. It’s time for a career you can be proud of. Join us.

STUDY DELIVERY SENIOR MANAGER (STUDY DELIVERY LEAD)

LIVE

What you will do

In this vital role, you will own global clinical trial delivery, translating product and clinical objectives into executable plans that ensure timely, high-quality data in support of Amgen’s mission to serve patients. You will own end-to-end delivery of assigned clinical studies with accountability for quality, timelines, budget, and operational performance, working across functions and geographies to drive consistent delivery.

  • Leading cross-functional study teams to deliver clinical data aligned with evidence generation strategy.
  • Defining and executing study plans covering feasibility, site selection, site engagement, recruitment, retention, and vendor delivery.
  • Identifying and managing study risks using quality-by-design and risk-based approaches to protect participant safety and data integrity.
  • Overseeing global study execution, including enrollment, data flow, monitoring, and corrective actions.
  • Providing clear leadership, issue resolution, and escalation management across geographies.
  • Partnering effectively with internal stakeholders and external vendors to ensure performance and collaboration.
  • Driving continuous improvement, innovation, and regulatory compliance throughout the study lifecycle.

WIN

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. What we seek in you as an experienced professional, are these qualifications and skills:

  • Degree educated
  • Clinical trial execution experience and previous people leadership managing teams, projects, resources or or directing the allocation or resources
  • Previous experience in life sciences or a related field, including biopharmaceutical clinical research
  • Previous management experience of direct reports across multiple geographies
  • Experience representing a sponsor company in regulatory audit/inspections
  • Experience at or oversight of outside clinical research vendors (CRO’s, central labs, imaging vendors, etc.)

THRIVE

What you can expect of us

As we work to develop treatments that take care of others, so we work to care for our teammates’ professional and personal growth and well-being.

  • Vast opportunities to learn and move up and across our global organization
  • Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
  • Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

LOCATION: Ability to work flexibly from home with regular office work either from our Cambridge or Uxbridge next generation workspace.

APPLY NOW

Objects in your future are closer than they appear. Join us.

careers.amgen.com

Equal Opportunity Statement

Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.

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