Associate Centralized Monitor - Poland

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Poland
Base: zł80,500.00 - zł149,500.00; bonus/equity: no...
Onsite
Centralized monitoring activities
Subject level data review
Clinical trial systems proficiency
Provide study level administrative support to the clinical study management team

Job Summary

  • Provide study level administrative support to the clinical study management team.
  • Perform centralized monitoring activities on assigned sites and evaluate their quality and integrity.
  • Facilitate early identification of site-level risk/issue(s) occurring during study conduct.

Matching Summary

Provide study level administrative support to the clinical study management team.

Salary

Base: zł80,500.00 - zł149,500.00; Bonus/Equity: Not specified; Benefits: Not specified

Skills & Requirements

Must-have

  • Centralized monitoring activities
  • Subject Level Data Review
  • Clinical trial systems proficiency
  • ICH-GCP knowledge
  • Monitor site performance

Nice-to-have

  • Results and detail-oriented
  • Problem-solving skills
  • Effective working relationships
  • Strong telecommunication skills

Key Requirements

  • 2 to 5 years of work experience
  • 1 year relevant experience
  • Graduate/Post Graduate in Life Sciences
  • Proficient in Clinical Systems (EDC, IXRS, CTMS)
  • Good command of English language
  • Good command of Czech and Slovak language

Work Rights

Not specified

Tailored Resume

Cover Letter