Caidya in the United States (Remote) is seeking a Clinical Research Associate II to monitor investigational sites across the trial lifecycle, ensuring subject safety, data quality, and regulatory compliance.
Have you got what it takes to succeed The following information should be read carefully by all candidates.
You will serve as the primary contact for sites, conduct on-site and remote monitoring visits, review regulatory files, manage data queries, and support study conduct with cross-functional xmvmafu teams while traveling up to 35%.
Remote working/work at home options are available for this role.