Support all day-to-day activities involved with research protocols. Assist with participant recruitment, primarily scheduling and consenting research participants. Assist CRC leads with data collection and data entry (adhering to proper protocols). Prepare study materials for each study protocol. Prepare and process biological specimens; etc. Perform study-related procedures under the direction of the study lead and/or manager, including administering questionnaires, performing phlebotomy, collecting nasal swabs and brushings, conducting sputum induction, and performing pulmonary function testing. Assist lead coordinators in contacting the investigational pharmacy to order, collect, and distribute the appropriate study pharmaceuticals, as needed. Maintain drug accountability and destruction logs, as required. Access appropriate electronic medical records (EMRs) as needed to confirm inclusion/exclusion of research participants and to log AE’s/SAE’s. Assist the regulatory team with monitoring visits: Prepare monitoring room prior to monitoring visits. Review and confirm study materials are available and complete. Escort monitor to A2DRC and restricted hospital areas, as appropriate and necessary. Provide requested documents to monitor throughout the visit. Assist with any actionable items following each site visit. Participate in health fairs, community events, workshops, and other development activities under the direction of the CRU Manager, as requested. Knowledge, Skills, and Abilities: Ability to travel as needed.