Associate Centralized Monitor - Poland

IQVIA Inc

Base: zł80,500.00 - zł149,500.00; bonus/equity: no...
Onsite
Centralized monitoring activities
Clinical trial management systems
Data review and analytics
IQVIA Inc is seeking an Associate Centralized Monitor in Poland to support clinical study management teams by performing administrative tasks, ensuring compliance with regulations, and assisting in centralized monitoring activities. The ideal candidate will have a background in life sciences, relevant experience in clinical research, and strong communication skills in English and local languages

Job Summary

  • Provide project related assistance to assigned project teams ensuring all work complies with SOPs, policies, good clinical practices, and regulatory requirements.
  • Perform centralized monitoring activities, data review, and site performance evaluation to identify risks and recommend corrective actions during clinical trials.
  • Support technical solution specialists with Excel tool automation and maintain effective communication with sites, CRAs, and project teams.

Matching Summary

Match Score: 85

IQVIA Inc is seeking an Associate Centralized Monitor in Poland to support clinical study management teams by performing administrative tasks, ensuring compliance with regulations, and assisting in centralized monitoring activities. The ideal candidate will have a background in life sciences, relevant experience in clinical research, and strong communication skills in English and local languages.

Salary

Base: zł80,500.00 - zł149,500.00; Bonus/Equity: Not specified; Benefits: Range of health and welfare and/or other benefits

Skills & Requirements

Must-have

  • Centralized monitoring activities
  • Clinical trial management systems
  • Data review and analytics
  • Project communication and coordination
  • Clinical data quality evaluation
  • Microsoft Office proficiency
  • Clinical regulatory compliance

Nice-to-have

  • Problem-solving skills
  • Time management and prioritization
  • Strong telecommunication skills
  • Experience with macros and Excel automation
  • Multilingual communication (English, Czech, Slovak)

Key Requirements

  • Graduate/Post Graduate in Life Sciences or related field
  • 2 to 5 years work experience with minimum 1 year relevant experience
  • Good knowledge of ICH-GCP and local regulations
  • Proficient in clinical systems such as EDC, IXRS, CTMS
  • Good command of English, Czech and Slovak languages

Work Rights

Not specified

Tailored Resume

Cover Letter