Essential Functions of the Job: Edit and submit study protocols and other required research documentationProvide information regarding respiratory pathogen prevention and testingRecruit and enroll study participants according to study protocolsObtain informed consent for all study participantsPerform data entry using the study data management system (e.g., REDCap, Access, EPIC)Performs or assists with routine data verification and quality controls to ensure data integrity and consistencyAssist in the setup, operation, and maintenance of research equipment and/or instrumentation as specifically instructedTrack research participants and perform follow-up tasks according to study protocolFollow study protocols (IRB, SOPs, MOPs), and adheres to study protocols, Good Clinical Practice (GCP), and ethical research principlesProvide assistance in a variety of tasks in support of established recruitment and retention goalsDemonstrate skills and abilities by following the guidelines in venipuncture, heel/finger stick, and/or saliva sample collectionProvide assistance to the Principal Investigator, Program Manager, and Program Supervisor as needed. Technical Knowledge and Skills Required to Perform the Job: Superb organizational ability and exceptionally analyticalAbility to work well in a fast-paced, deadline driven, collaborative environmentProficiency in administrative skills and time managementExperience and knowledge with Microsoft.