A leading life sciences recruitment agency is seeking an experienced Clinical Research Coordinator for a freelance onsite project in Poland. You will play a pivotal role in eCRF completion, site file management, and supporting the Principal Investigator in critical clinical studies. The ideal candidate must have prior experience in clinical trials, strong organizational skills, and the ability to manage multiple tasks efficiently. This role offers up to 32 hours per week, depending on project needs and recruitment progress.
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