Senior Clinical Research Associate, Sponsor Dedicated In Poland

IQVIA UK

Poland
Base: 171,900.00 zł - 375,700.00 zł; bonus/equity:...
Fully remote
3+ years on-site monitoring experience
Strong knowledge of gcp and ich guidelines
Fluency in polish and english languages
This role offers the stability of a global CRO while providing direct experience with leading pharma clients

Job Summary

  • This role offers the stability of a global CRO while providing direct experience with leading pharma clients.
  • Responsibilities include performing site selection, initiation, monitoring, and close-out visits to ensure regulatory compliance.
  • The position includes benefits such as a company car, home-office setup, and flexible work schedules.

Matching Summary

This role offers the stability of a global CRO while providing direct experience with leading pharma clients.

Salary

Base: 171,900.00 zł - 375,700.00 zł; Bonus/Equity: Incentive plans may be offered; Benefits: Health, welfare, company car, home-office

Skills & Requirements

Must-have

  • 3+ years on-site monitoring experience
  • Strong knowledge of GCP and ICH guidelines
  • Fluency in Polish and English languages

Nice-to-have

  • Experience with remote monitoring
  • Therapeutic area specialization
  • Study start-up process involvement

Key Requirements

  • University degree in life science or health care apprenticeship
  • Minimum 3 years of clinical trial monitoring experience
  • Good command of Polish and English language

Work Rights

Not specified

Tailored Resume

Cover Letter