Sr. Clinical Trial Specialist, Poland

Exact Sciences

Warsaw, , Poland
Base: 173,000,00 zł - 284,000,00 zł; bonus/equity:...
Clinical study operations management
Clinical research regulations adherence
Cro and vendor oversight
The Sr. Clinical Trial Specialist, Poland will be part of the Clinical Affairs Team responsible for planning, executing, managing and closing projects associated with the company clinical study plans

Job Summary

  • The Sr. Clinical Trial Specialist, Poland will be part of the Clinical Affairs Team responsible for planning, executing, managing and closing projects associated with the company clinical study plans.
  • This role requires managing day-to-day operations of assigned clinical studies, ensuring successful execution of clinical research plans, and supporting multidisciplinary project teams internally and externally.
  • Exact Sciences fosters a culture where all employees can develop personally and professionally with a sense of respect and belonging.

Matching Summary

The Sr. Clinical Trial Specialist, Poland will be part of the Clinical Affairs Team responsible for planning, executing, managing and closing projects associated with the company clinical study plans.

Salary

Base: 173000,00 zł - 284000,00 zł; Bonus/Equity: discretionary bonus possible; Benefits: robust benefits to support your life

Skills & Requirements

Must-have

  • clinical study operations management
  • clinical research regulations adherence
  • CRO and vendor oversight
  • clinical protocol implementation
  • project scope and timeline management
  • document standardization and peer review

Nice-to-have

  • cross-functional team collaboration
  • problem-solving and interpersonal skills
  • fast-paced environment adaptability
  • multilingual communication skills
  • quality management system compliance
  • customer advocacy throughout project lifecycle

Key Requirements

  • Bachelor’s degree in life sciences
  • Minimum 5 years clinical research experience
  • At least 1 year sponsor/CRO clinical research experience
  • Fluency in English (C1 or above)
  • Authorized to work in Poland
  • Knowledge of Good Clinical Practices and US regulations
  • Experience with FDA submission processes

Work Rights

Must be authorized to work in Poland

Tailored Resume

Cover Letter