Clinical Site Contracts Controller

BeiGene

Remote
Base: $136,400.00 - $181,400.00 annually; bonus/eq...
Cost per patient modeling
Budget benchmarking
Data-driven budget insights
The Clinical Site Contracts Controller is a strategic analytics and governance role focused on strengthening budget analysis, enhancing cost per-patient (CPP) library utilization, and ensuring consistent, data-driven budget decision support

Job Summary

  • The Clinical Site Contracts Controller is a strategic analytics and governance role focused on strengthening budget analysis, enhancing cost per-patient (CPP) library utilization, and ensuring consistent, data-driven budget decision support.
  • This role enables faster negotiations by providing objective budget insights while preserving execution ownership within the Contracts team, and involves leading advanced analysis of site budgets against CPP benchmarks and country guardrails.
  • The company offers a comprehensive benefits package including Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness, with opportunities for bonus, equity, and stock purchase plans.

Matching Summary

The Clinical Site Contracts Controller is a strategic analytics and governance role focused on strengthening budget analysis, enhancing cost per-patient (CPP) library utilization, and ensuring consistent, data-driven budget decision support.

Salary

Base: $136,400.00 - $181,400.00 annually; Bonus/Equity: Eligible for annual bonus plan and discretionary equity awards; Benefits: Comprehensive benefits package

Skills & Requirements

Must-have

  • cost per patient modeling
  • budget benchmarking
  • data-driven budget insights
  • advanced Excel and data analytics
  • clinical trial contracting process

Nice-to-have

  • highly motivated
  • collaborative
  • passionate interest in fighting cancer
  • executive communication skills
  • governance mindset

Key Requirements

  • Bachelor’s degree or 7+ years experience
  • Life Sciences, Business, Finance, Health Economics background
  • Experience in clinical site budgets, contracts, or study start-up
  • Proficiency in Microsoft Office apps, PowerBI, CTMS, CLM systems
  • Understanding of ICH-GCP and pharmaceutical regulations

Work Rights

Not specified

Tailored Resume

Cover Letter