Experienced Clinical Research Associate, Site Management Poland

Our team is growing, join us on our mission to drive healthcare forward! 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 to enhance predictability - Administer protocol and…