Research Technician II

Tucson, AZ, US April 25, 2026
Screen and evaluate subjects for inclusion into clinical trials, ensuring potential participants meet eligibility criteria by communicating with the treatment team and/or investigator. Explain trial to participant and their families, obtain consent, and enroll participants into the study. Schedule and/or perform medical testing per protocol such as coordinating imaging, drawing blood, sample processing laboratory samples. Assess and follow patients throughout study protocols and follow-up. Maintain protocol compliance. Complete case report forms by entering data into electronic database for study participants. Maintain and organize participant data. Administers and assists in the coordination of assigned programs and projects in addition to primary study. Conduct psychometric assessments of enrolled subjects as directed by research protocol after completing training and certification. Submit study protocols and amendments, consent forms, and recruiting materials to the Institutional Review Board and department for approval with oversight from supervisor. Provide team coordination, communication, and quality control. Works with division faculty to develop compliance forms and tracking documents. Attend site visits, and various other duties or projects as assigned. Assist in training lower-level staff and student research associates. Mentors and shares knowledge with student workers. Experience training or mentoring junior lab members preferred.
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