Assist study providers with adverse event monitoring and reporting Perform clinical procedures, in collaboration with study providers, that includes but is not limited to: obtaining vital signs, administering injections, performing symptom-directed physical exams, collecting detailed health histories, conducting sexual health risk-reduction counseling, performing electrocardiograms, and sample collection (i.e., venous blood; oral, anal, and genital cultures; and urine/stool/tissue specimens) Start and maintain peripheral intravenous lines Assist providers in assessing, interpreting, and communicating laboratory results to the participant Translate clinical information for non-clinical research staff (e.g., study coordinators and research associates) Maintain the emergency crash cart on the research floor Assist the Non-Clinical Team with Participant Interaction and Data Collection Obtain informed consent: Explain study procedures and risks/benefits to participants. Meets Agency Participatory Expectations Adheres to all agency and departmental policies and procedures Identifies potential or actual unsafe situations in the environment and takes measures to rectify the situation Attends all required meetings, in-services and professional trainings Maintains professional competence necessary to perform job responsibilities; maintains and provides agency with records of continuing education activities Serves on agency committees and in professional organizations when requested Work harmoniously and effectively with colleagues, patients, clients and vendors across the spectrum of diversity, including but not limited to race, ethnicity, color, gender identity, sexual orientation, age, socio-economic status, national origin and immigrant status, religious or spiritual identity, disability (physical, mental, emotional and developmental), veteran status, and/or limited English proficiency.