Research Assistant II, General Internal Medicine

Research Assistant II will support multi-site research focused on substance use and infectious disease across community, clinical, and carceral settings. The role manages daily and administrative research study functions, including participant recruitment and enrollment, data quality oversight, and compliance support.

• Administrative aspects of research studies and program records
• Assist with reports, presentations, and data analysis
• Recruit and enroll study participants including informed consent and randomization
• Review data collection forms and provide technical guidance for data entry
• Support IRB approvals and track/report adverse events

The position involves clinical research operations: administering enrollment workflows (including informed consent and randomization), conducting literature searches, collecting and reviewing study data forms, supporting data entry quality, and tracking adverse events in alignment with Institutional Review Board (IRB) requirements.

The ideal candidate is a Research Assistant II with experience supporting multi-site clinical research studies, including participant enrollment, informed consent, and randomization procedures. They can manage daily research administration, maintain data quality through data collection and data entry checks, and support IRB submissions and adverse event tracking. Strong communication and comfort interacting with participants, coordinators, and investigators are essential.