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Amgen

R&D Supplier Governance Manager

Amgen

Support R&D supplier governance for Amgen's global clinical trials while ensuring oversight of suppliers. Collaborate with internal stakeholders for process improvement in a dynamic clinical research environment.

Posted 7/10/2026full-timeRemote • 🇺🇸 United StatesMid-LevelSenior💰 $100,564 - $136,057 per yearWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in supplier governance and oversight within clinical trials, with a strong focus on performance measurement, risk management, and compliance with regulatory standards. Proven ability to collaborate with cross-functional teams and maintain relationships with key stakeholders in the life sciences sector.

Highest-signal resume keywords
Supplier GovernanceClinical Trial ExperienceGood Clinical Practices (GCP)FDA RegulationsPerformance Measurement

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Clinical Trial ManagementRegulatory ComplianceRisk ManagementPerformance ReportingProcess Improvement
Soft Skills
CollaborationRelationship BuildingCommunication
Tools & Technologies
Performance IndicatorsLogistics Management
Industry Keywords
Life SciencesBiopharmaceuticalsCE Marking510(k) ClearanceInternational Regulatory Requirements

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • Support Amgen sponsored clinical trials globally, reporting to the Sr. Manager of R&D Supplier Governance
  • Ensure appropriate governance and oversight of equipment and ancillary suppliers
  • Collaborate with senior management, and partner with internal stakeholders and suppliers for process improvement
  • Potentially up to 20% travel domestic and/or international
  • Measuring supplier performance and reporting performance feedback to internal partners and suppliers
  • Facilitating and implementing supplier governance meetings, operating reviews, monitoring key performance indicators, risk management and mitigation and performing issue management
  • Build and maintain relationships with key internal and external partners, including study teams, functional leads, procurement, quality, compliance, and suppliers

Requirements

What you’ll need
  • Doctorate degree OR Master’s degree and 2 years of relevant experience OR Bachelor’s degree and 4 years of relevant experience OR Associate’s degree and 8 years of relevant experience OR High school diploma / GED and 10 years of relevant experience
  • 7 years work experience in life sciences or medically related field, including 4 years of biopharmaceutical clinical trial experience
  • Experience with CE marking, 510(k) clearance, and other device regulation requirements.
  • Experience with customs (import/export) and logistics.
  • Knowledge of Good Clinical Practices (GCP), FDA regulations and guidelines, and international regulatory requirements/guidelines.

Benefits

Comp & perks
  • A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions
  • group medical, dental and vision coverage
  • life and disability insurance
  • flexible spending accounts
  • A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
  • Stock-based long-term incentives
  • Award-winning time-off plans
  • Flexible work models where possible.