The Clinical Research Specialist (CRS) is responsible for supporting and/or conducting clinical study activities and basic data collection at clinical sites, as well as managing assigned clinical projects & operations, including pre-monitoring activities, data entry, inventory management, device procurement, shipping, and financial management. Supports CRAs with IRB submissions, site training, tracking study progress and performance, and generating reports which includes interacting and communicating with site staff and key study personnel. Ensures all activities are conducted in accordance with regulations (FDA, EU MDR, and other international regulations), Good Clinical Practices (GCP), department standard operating procedures, and Masimo’s guiding principles including Masimo’s code of conduct and highest ethics.
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Education Level
Bachelor's degree
Number of Employees
1,001-5,000 employees