Senior Clinical Research Associate, Sponsor Dedicated In Poland

IQVIA

Poland
Base: 171.900,00 zł - 375.700,00 zł; bonus/equity:...
**
Site selection, initiation, monitoring, close-out
Evaluate site practices gcp ich
Manage progress tracking submissions
** IQVIA is seeking a Senior Clinical Research Associate (CRA) for a fully remote role in Poland, emphasizing collaboration with pharmaceutical companies and career growth. The position requires a minimum of three years of on-site monitoring experience and offers comprehensive training and development opportunities. **

Job Summary

  • When you join IQVIA as a sponsor-dedicated Senior CRA in Poland, you’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our clients.
  • Your responsibilities will include performing site selection, initiation, monitoring and close-out visits and managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolution.
  • We invite you to join IQVIA™ and can expect resources that promote your career growth, leaders that support flexible work schedules, and programs to help you build your therapeutic knowledge.

Matching Summary

Match Score: 75

** IQVIA is seeking a Senior Clinical Research Associate (CRA) for a fully remote role in Poland, emphasizing collaboration with pharmaceutical companies and career growth. The position requires a minimum of three years of on-site monitoring experience and offers comprehensive training and development opportunities. **

Salary

Base: 171.900,00 zł - 375.700,00 zł; Bonus/Equity: Not specified; Benefits: Not specified

Skills & Requirements

Must-have

  • site selection, initiation, monitoring, close-out
  • evaluate site practices GCP ICH
  • manage progress tracking submissions
  • collaborate with site experts client representatives
  • strong written verbal communication skills
  • good command of Polish English

Nice-to-have

  • intentional career growth professional development
  • world-class training mentoring
  • gain experience wide variety therapeutic areas
  • flexibility to travel

Key Requirements

  • minimum 3 years on-site monitoring experience
  • strong experience monitoring clinical trials
  • knowledge applicable clinical research regulatory requirements
  • university degree life science scientific discipline
  • apprenticeship in health care

Work Rights

Not specified

Tailored Resume

Cover Letter