The Cytogenetic Analyst will perform routine and complex technical procedures according to departmental Standard Operating Procedures, monitor equipment, and report accurate test results. Responsibilities include analyzing chromosomes, reviewing test requisitions, summarizing results using ISCN nomenclature, and distinguishing between normal and abnormal results.
Join our team in Italy as an experienced CRA II or Senior CRA, where you'll monitor oncology clinical studies. This remote position offers reasonable travel and work/life balance. You'll ensure studies are conducted per protocol, SOPs, and regulations, and contribute to study setup, investigator identification, and regulatory submissions. Your voice will be heard in this smaller CRO.
Monitor and own the progress of clinical studies at investigative sites, ensuring clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. Coordinate activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions, conducting pre-study and initiation visits, etc.).