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 17, 2020
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.
March 25, 2020
Works cooperatively and productively in a multi-disciplinary organization, which includes primary care, mental health, and other health and wellness programs.
April 06, 2020
Prepare and/or generate final statistical reports using a computer and independently interpret research data.
April 21, 2020
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).
April 22, 2020
Graduate of an approved discipline specific program (or equivalent experience) and < 1 year of experience.
May 19, 2020
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.
May 27, 2020