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Amgen

Makes biotech medicines for serious illnesses

Global Category Lead - Multiple Teams

Procurement & SourcingConfirmed live in the last 24 hours
Full-timeRemote in USARemote

About the Job

Requirements

  • Doctorate degree and 3 years of global strategic sourcing or procurement experience; or master's degree and 5 years; or bachelor's degree and 7 years; or associate's degree and 12 years; or high school diploma/GED and 14 years.
  • Familiarity with procurement platforms such as Ariba, ERP systems, and advanced analytics tools.
  • Strong analytical skills, including analyzing large datasets, identifying trends, and deriving actionable insights.
  • Experience leading cross-functional teams and managing complex global projects in a matrixed environment.
  • Familiarity with compliance frameworks such as 21 CFR Part 11, GxP, HIPAA, and GDPR.
  • Extensive knowledge of the global vendor landscape supporting clinical trials, including Contract Research Organizations, Site Management Organizations, Academic Medical Centers, and CRO-adjacent vendors.
  • Global category management experience with a record of executive business partnering, leading change, and enterprise activation of sourcing initiatives based on marketplace expertise.
  • Deep understanding of category management principles, supplier relationship management, and contract lifecycle management.
  • Financial, legal, and contractual fluency for navigating sales services agreements and delivering business-aligned outcomes.
  • Experience driving innovation in category strategy development, supplier engagement models, and internal stakeholder partnerships.
  • Ability to communicate complex category strategies, influence senior stakeholders, and manage change across functions and regions.
  • Ability to leverage spend analytics and benchmarking to inform category strategies and uncover value opportunities.
  • Understanding of regulatory landscapes and ability to manage compliance requirements.
  • Ability to partner with Legal, Compliance, Cybersecurity, and Regulatory Affairs.
  • Contractual and regulatory navigation skills for healthcare technology agreements.

Responsibilities

  • Lead category management for Full-Service CRO, supporting all phases of fully outsourced clinical trials, including ClinPharm, Phases I–IV, Observational Research, and inherited studies resulting from mergers and acquisitions.
  • Partner with R&D, Clinical, Regulatory, and Compliance teams to align with FDA, EMA, HIPAA, and GCP standards.
  • Negotiate contracts, amendments, commercial terms, rates, and discounts with vendors supporting fully outsourced clinical trials, balancing innovation with compliance and risk.
  • Partner with Program Leads, Study Teams, and R&D Supplier Governance to enable supplier governance frameworks, drive high-quality delivery and performance, and resolve issues effectively and promptly.
  • Monitor market trends and intelligence, including evolving digital health regulations, and integrate compliance, quality, and risk mitigation into sourcing strategies.
  • Provide strategic oversight as lead for the Full-Service CRO category and sourcing, aligning category strategies with business needs and organizational objectives.
  • Facilitate collaboration across cross-functional teams and regional stakeholders to ensure procurement strategies meet organizational needs and are implemented effectively.
  • Ensure procurement activities supporting Full-Service CRO comply with regulatory, contractual, and operational risk requirements; partner with Legal, Compliance, Data Privacy, and Cybersecurity on risk mitigation and best practices.
  • Collaborate with Global Procurement colleagues and stakeholders on complex negotiations for CRO master services agreements and amendments, including support for study-level agreements and purchase orders, and provide guidance on RFPs, supplier evaluations, and contract development.
  • Activate procurement resources and facilitate delegation of sourcing activities to advance category priorities, manage stakeholder expectations, and mitigate risk.

Desired Qualifications

  • Excellent problem-solving and organizational skills.

About the Company

Amgen

Makes biotech medicines for serious illnesses

Amgen develops and makes biologic medicines, which are drugs built from proteins and antibodies grown in living cells, for serious conditions such as heart disease, cancer, and bone loss. Its anemia drug Epogen, approved in 1989, became one of the biotechnology industry's first blockbuster medicines. Amgen grows these drugs in large tanks called bioreactors, and its products include the cholesterol drug Repatha, the bone-building drug Evenity, and the severe asthma drug Tezspire. It earns money by selling these medicines, mostly through large drug wholesalers that supply hospitals and pharmacies. Amgen was founded in 1980 and is based in Thousand Oaks, California.

Company size
10,001+
Company stage
IPO
Headquarters
Thousand Oaks, CA
Founded
1980

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