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Clinical Research Associate, Single Sponsor dedicated in POLAND
2 tygodni temu
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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