Clinical Research Associate I/ Clinical Research Associate II

Monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. Coordinate all necessary activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions, conducting pre-study and initiation visits, etc.). This role requires at least one year of CRA experience (including 6 months of independent monitoring) within the CRO or pharmaceutical industry and availability for domestic travel including overnight stays, which may constitute up to approximately 50-60% travel commitment.