Clinical Research Associate , Multisponsor Team
IQVIA
IQVIA seeks a Clinical Research Associate for its multisponsor team in Bucharest to conduct clinical trial visits and site support across Romania. The role involves monitoring study progress, managing documentation, and ensuring compliance with ICH-GCP guidelines.
Responsibilities
- Conduct site visits including selection, initiation, monitoring, and close-out activities
- Support patient recruitment at study sites
- Manage root cause analyses and corrective action plans
- Document visit findings in monitoring reports and follow-up correspondence
- Maintain and archive study documentation in electronic trial master file systems
Requirements
- Master's or Bachelor's degree in Health Sciences or related field
- Minimum 1 year experience as a Clinical Research Associate
- Proficient in Romanian and English languages
- Strong knowledge of ICH-GCP guidelines and application
- Experience with CTMS, eTMF, and EDC systems
- Exposure to multiple study phases, visit types, and therapeutic areas
- Valid driving license and ability to travel throughout Romania
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