Summary from listing
This one-year term appointment provides research, data analysis, and operational support to principal investigators and research coordinators for clinical research studies. Responsibilities include participant recruitment and eligibility assessment, consent protocol support, literature reviews, study database creation and data entry, qualitative coding and thematic analysis, statistical analysis, IRB or IACUC submissions, and grant documentation. A high school diploma is required, a bachelor's degree is preferred, and approximately one year of related experience is requested; SPSS or RedCap experience is required, while clinical research and medical terminology knowledge are helpful.
