-Responsible for startup activities including delegation logs, training logs, SIV, etc.-Identification and recruitment of potential study subjects. -Collect used IP and dispense new IP (IVRS)-Make source documents to collect study data-Enter confidential patient data in EDC and answer queries-Take vital signs, conduct ECG, draw blood-Prepare for monitor visits – verify source – ensure all data is complete and entered into EDC. -Resolve all queries.-Meet and work with CRA to correct data on the day of monitoring visit.-Facilitates training of all applicable personnel.-Oversees any work by the research assistant or other personnel involved in the trial.

-Promoted from an intern to Research Assistant role in October -Prepare charts, prepare lab shipments, and prep for the day-Promote upcoming studies and assist with recruitment-Conduct subject visits under supervision of coordinator

-Supervised 3-5 employees