Create and manage databases for studies, which includes setting up database and associated data entry programs and retrieving data from database for purposes of analyses or data review.
July 26, 2021
Serves as an advocate for human subjects by establishing and maintaining communication with Investigators, research staff, Sponsors, participants and representatives of professional organizations, participant advocates, and the public responsible for, or concerned about, protections for human participants of research.
October 30, 2021
Participates in the ongoing informed consent process, ensuring that human subjects, their families, and other health care providers clearly understand what is expected of and from them in the course of participating in a clinical trial.
November 09, 2021
Assist faculty researchers or may act independently, in the planning and designing of research projects, establishing priorities and recommending schedules and timetables.
November 21, 2021
Monitors vaccine supplies, currency and supplies of vaccine information materials.
December 14, 2021
Graduate of an approved discipline specific program (or equivalent experience) and < 1 year of experience.
December 21, 2021
Performs procedures for research as they are described in the protocol, deviating from the protocol only when a subject's safety is at risk and reports all deviations from the protocol to the Principal Investigator and/or senior personnel who will determine of a protocol amendment or other safety assessments are required.
January 13, 2022