Sr. Clinical Affairs Specimen Operations Manager

175

Madison, WI, US
Base: $91,000.00 - $155,000.00; bonus/equity: bonu...
Not specified (assumed to be in-office due to location)
7+ years clinical trial operations experience
3+ years project management support role
Bachelor's degree in health or life sciences
Exact Sciences is seeking a Sr. Clinical Affairs Specimen Operations Manager in Madison, WI, to oversee specimen logistics for clinical studies, ensuring operational efficiency and regulatory compliance. The role demands extensive experience in clinical trial operations, logistics, and project management. ###

Job Summary

  • This role leads the strategic management of specimen logistics to ensure reliable study delivery aligned with business objectives.
  • The position requires translating complex study requirements into actionable plans while managing key performance metrics like sample quality and turnaround times.
  • Exact Sciences offers a robust benefits package including paid time off, parental leave, and comprehensive health coverage for this purpose-driven career.

Matching Summary

Match Score: 85

Exact Sciences is seeking a Sr. Clinical Affairs Specimen Operations Manager in Madison, WI, to oversee specimen logistics for clinical studies, ensuring operational efficiency and regulatory compliance. The role demands extensive experience in clinical trial operations, logistics, and project management. ###

Salary

Base: $91,000.00 - $155,000.00; Bonus/Equity: Bonus eligible; Benefits: PTO, parental leave, retirement savings, medical/dental/vision

Skills & Requirements

Must-have

  • 7+ years clinical trial operations experience
  • 3+ years project management support role
  • Bachelor's degree in health or life sciences
  • Cross-functional coordination of specimen logistics
  • Knowledge of FDA regulations and ICH GCP

Nice-to-have

  • Process and workflow design experience
  • CAPM certification through PMI
  • Global regulatory understanding
  • Inclusion mindset and teamwork values
  • Experience with clinical systems functionality

Key Requirements

  • Bachelor's degree in relevant field
  • 7+ years in clinical trial operations
  • 3+ years in project management support
  • Understanding of FDA and ICH GCP regulations

Work Rights

Not specified

Tailored Resume

Cover Letter