R&D Supplier Governance Senior Associate, PO Management

Amgen Inc.

3.6

(9)

Hyderabad, India

Why you should apply for a job to Amgen Inc.:

  • 67% say women are treated fairly and equally to men
  • 78% would recommend this company to other women
  • Ratings are based on anonymous reviews by Fairygodboss members.
  • Flexible work models that empower staff members to work where and when they are most productive
  • Award-winning PTO plan and bi-annual company-wide shutdowns
  • With 11 Employee Resource Groups, 60 chapters & 11000 members everyone has opportunity to connect, network & foster a culture of belonging
  • #R-240406

    Position summary

    • Serve as counterpart for key clinical trial suppliers with respect to financial oversight working across the Amgen portfolio.

    • Maintain relationships with key suppliers to ensure process alignment, status updates and timely issue management.

    • Communicates, resolves, and tracks PO budget-related questions between Finance Operations and Clinical Trial teams

    • Maintains materials for project financial review meetings with Clinical study teams.

    • Maintain PO accuracy and compliance with Amgen policies

    • Maintain PO and SOW documentation in central repositories (e.g. TMF) and ensure audit/readiness standards are met.

    • Oversee timely review and approval of invoices in Amgen ERP system to ensure on time payments

    • Manage and resolve issues related to supplier invoices and payments in partnership with invoice approvers and Amgen AP

    • Maintain PO tracking (dashboard/log) and deliver regular PO status reports.

    • Monitor PO-related supplier delivery and identify PO risks; share issues with manager and Supplier Governance Leads for oversight and escalation.

    • Ensure PO activities align with GCP, company procurement policies and clinical trial requirements.

    Key Activities

    • PO lifecycle management

      • Review SOWs to confirm compliance with Amgen purchasing standards.
      • Prepare and submit PO and funding requests through the enterprise procurement/P2P system or established finance workflow; follow up until submission confirmation.
      • Manage PO amendments and change orders to reflect scope changes.
    • PO submission & tracking

      • Submit POs via the enterprise procurement/P2P or finance workflow and maintain a PO tracking dashboard showing submission, routing/approvals, funding status, and closure targets.
      • Proactively chase routing/processing issues and escalate blockers to the Manager or Supplier Governance Leads
      • Analyze PO related data support optimized processing times and quality
      • Communicate on a regular basis with supplier and Amgen stakeholders regarding progress of pending PO requests and to monitor PO budgets
    • Financial stewardship ( PO spend tracking)

      • Perform ongoing budget reviews and track commitments against PO balances; identify variances and forecast spend related to active clinical supplier POs.
      • Provide accurate and complete supplier PO information to support financial accrual and forecasting processes
      • Perform data QC to ensure accuracy of data in source systems
      • Use data analysis to investigate issues, answer study budget related queries
    • Supplier oversight & issue coordination

      • Monitor supplier delivery versus PO/SOW milestones and summarize PO-related risks for stakeholders.

      • Communicate with supplier and study teams to review PO, invoice, and PO budgets topics

      • Independently manage and resolve issues related to SoW, PO and invoices to support clinical trial execution and budget management.

      • Manage multiple priorities, balancing study delivery and budgetary controls to ensure timely execution of SoW/POs and timely invoice approval.

      • Ensure PO/SOW linkage to TMF and central repositories is maintained and audit-ready

    Basic Qualifications

    • Bachelor's degree (preferred: scientific degree or RN) or equivalent experience.

    • 5-9 year experience in PO management, preferably within clinical research, CRO, biotech or pharmaceutical settings.

    • Demonstrated experience with PO/SOW management and clinical supplier budgets.

    • Experience working in a global matrix environment is preferred.

    Preferred Qualifications

    • Biopharmaceutical clinical research experience (clinical research experience obtained working on clinical trials at a biotech, pharmaceutical or CRO company)

    Knowledge

    • Knowledge working in a global, matrix organization

    • Knowledge of Good Clinical Practice (GCP)

    • Strong organizational and project management skills; able to manage competing priorities

    • Strong Proficiency with enterprise procurement/P2P workflows, Microsoft Office Word, Excel and SharePoint

    • Excellent understanding of financial concepts and analytical skills

    • Financial acumen sufficient for budgeting, forecasting and PO balance monitoring.

    • Clear written and verbal communication; ability to coordinate cross-functional stakeholders.

    • Problem-solving orientation and appropriate escalation judgment.

    • Professional collaboration skills

    .

    Why you should apply for a job to Amgen Inc.:

  • 67% say women are treated fairly and equally to men
  • 78% would recommend this company to other women
  • Ratings are based on anonymous reviews by Fairygodboss members.
  • Flexible work models that empower staff members to work where and when they are most productive
  • Award-winning PTO plan and bi-annual company-wide shutdowns
  • With 11 Employee Resource Groups, 60 chapters & 11000 members everyone has opportunity to connect, network & foster a culture of belonging