Clinical Research Associate, Single Sponsor dedicated in POLAND

2 tygodni temu


Warszawa, Mazovia, Polska Pharmiweb Pełny etat

IQVIA is looking for Clinical Research Associates

Join IQVIA now and have a positive influence on patients' well-being.

Job Summary
Execute monitoring and site management tasks to ensure sites comply with the study protocol, regulations, guidelines, and sponsor specifications.

Duties

  • Conduct site selection, initiation, monitoring, and close-out visits while maintaining accurate documentation
  • Assist in creating a subject recruitment strategy
  • Establish ongoing communication channels and provide protocol and study-related training to assigned sites
  • Assess site practices for quality and integrity – escalate any quality issues as necessary
  • Oversee progress by monitoring regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution

Requirements

  • Hold a Bachelor's degree in a healthcare or scientific field or equivalent education
  • Experience in on-site monitoring of clinical trials
  • Alternatively, possess a similar mix of education, training, and practical experience
  • Strong written and verbal communication skills, including fluency in Polish and English

Seize this exciting opportunity

IQVIA strongly supports workplace diversity and inclusion. We are firm believers that an inclusive work environment enhances our competitive edge in the global market and fosters success. Our culture of respect and inclusivity promotes team cohesion, nurtures individual potential, and strengthens our workforce. Join us and be part of shaping a healthier world.



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