Experienced Clinical Research Associate (Senior / CRA II)

Act as the main line of communication between the project team, sponsor, and the site while building relationships with site staff. Prepare, conduct, and report site selection, initiation, routine monitoring, and close-out visits to ensure subject recruitment targets and project timelines are met. Manage adverse events, protocol deviations, source data verification, and data queries at the site level. Ensure proper handling of investigational products, reconcile study documents and Investigator Site Files, and conduct audit preparation visits. Facilitate document flow between the project team, site, and central laboratory, and conduct project-specific training of site investigators. Maintain study-specific and corporate tracking systems and support regulatory submission packages. Requires at least two years of independent on-site monitoring experience in Israel, proficiency in Hebrew and English, and a valid driver's license.