Sr. Analyst Ii, Clinical Program Sourcing & Contracting Management (cpscm)

Biogen

Warsaw, Poland
Base: zł122,000.00-zł163,250.00; bonus/equity: ann...
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End-to-end study-level sourcing
Contracting activities for global clinical trials
Negotiate scope and pricing
** Biogen is seeking a Sr. Analyst II for Clinical Program Sourcing & Contracting Management in Warsaw, Poland. The role involves managing end-to-end sourcing and contracting activities for global clinical trials, primarily focusing on vendor service categories under established agreements, while ensuring compliance and operational efficiency. **

Job Summary

  • As the Sr. Analyst II in Clinical Program Sourcing & Contracting Management (CPSCM), you will be pivotal in executing end-to-end study-level sourcing and contracting activities for global clinical trials, spanning from Phase I to IV.
  • Your role ensures documentation accuracy, system integrity, and inspection readiness, playing a critical part in delivering compliant, efficient, and predictable contracting outcomes.
  • Competitive Total Rewards include base salary, annual bonus, life insurance, pension program contributions, mental health resources, remote work allowance, and flexible work arrangements.

Matching Summary

Match Score: 75

** Biogen is seeking a Sr. Analyst II for Clinical Program Sourcing & Contracting Management in Warsaw, Poland. The role involves managing end-to-end sourcing and contracting activities for global clinical trials, primarily focusing on vendor service categories under established agreements, while ensuring compliance and operational efficiency. **

Salary

Base: zł122,000.00-zł163,250.00; Bonus/Equity: annual bonus; Benefits: life insurance, pension program contributions, mental health resources, remote work allowance, flexible work arrangements

Skills & Requirements

Must-have

  • end-to-end study-level sourcing
  • contracting activities for global clinical trials
  • negotiate scope and pricing
  • execute Statements of Work (SOWs)
  • adhere to MSAs and internal controls

Nice-to-have

  • disciplined compliance mindset
  • analytical approach to pricing
  • continuous improvement
  • collaborating within matrix organizations

Key Requirements

  • Bachelor’s degree required
  • 3–5+ years of experience
  • Foundational understanding of clinical trial vendor models
  • Experience drafting or supporting SOWs
  • Holder of work permit & residency in Poland

Work Rights

Work permit & residency required

Tailored Resume

Cover Letter