Orient, train or teach, and give work direction to new researchers on the projectCoordinate studies across collaboratorsAct as a resource to other staff regarding study protocol and interpretationsResponsible for regulatory compliance in conjunction with the PI by providing study materials requested including, but are not limited to:Develop and maintain project materials (e.g., patient database, case report forms, study worksheets, tracking logs, IRB required forms, etc.)Accurately write and revise clinical protocols, consents, and other supporting documents Assist the Principal Investigator with reaching project milestones and resource allocation to assure successful study conductOversee progress and assure milestones are met for the research activities conducted by collaborators at external academic institutionsOrganize, and coordinate meetings, conference calls, and training sessionsManagement of patient advisory groupConsult with the Principal Investigator and co-investigators on appropriate management of participant problems and concerns. ESSENTIAL JOB FUNCTIONS: Responsible for managing tasks associated with participant screening, recruitment, and engagement in research projects, which includes, but is not limited to:Determining participant eligibilityRecruitmentTracking enrollment dates and key patient milestonesCoordinates/conducts research participant testing and follow-up.