Experienced Clinical Research Associate, Site Management Poland
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Opportunity in a dynamic multi‑sponsor environment - we are looking for experienced CRAs for our Site Management Team in Poland!
Responsibilities
Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory
requirements
, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Work with sites to adapt, drive, and track subject recruitment plan in line with project needs…
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