Monitors vaccine supplies, currency and supplies of vaccine information materials.
December 10, 2022
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.
February 26, 2023
Graduate of an approved discipline specific program (or equivalent experience) and < 1 year of experience.
March 12, 2023
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.
March 13, 2023
Understands and is capable of performing the procedures required of each study protocol (obtains training needed to safely and accurately perform or assess required procedures).
March 29, 2023
Assist faculty researchers or may act independently, in the planning and designing of research projects, establishing priorities and recommending schedules and timetables.
March 30, 2023
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.
April 01, 2023
Prepare and/or generate final statistical reports using a computer and independently interpret research data.
April 01, 2023
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.
April 18, 2023
Works cooperatively and productively in a multi-disciplinary organization, which includes primary care, mental health, and other health and wellness programs.
April 27, 2023
