Manages daily operations of research study involving multidisciplinary teams of colleagues, sponsors & other external project stakeholders. Monitors study performance, analyzes & review results, & supervises development & implementation of new protocols. May assign work & supervise study staff & reviews technical operations ensuring that all processes, protocols & procedures are quality controlled & functioning up to standards.

This position is responsible for overseeing, organizing and implementing multiple clinical research trials being conducted .This individual ensures appropriateness of patients supervises data collection and reporting, patient management and ensures adherence to all regulatory requirements and sponsor protocols. In addition, this individual will act as a resource to research study patients, physicians and other clinic personnel.

Data Entry, Data Migration, Query Resolution, Adverse Event Monitoring, Informed Consents, Patient Recruitment, Scheduling patient appointments, Chart review, administrative tasks.

Must have: 2 years of experience within clinical research