_Equivalent education/experience will substitute for all minimum qualifications except when there are legal requirements, such as a license/certification/registration._ **ADDITIONAL REQUIREMENTS** + Experience as a clinical study coordinator working with study participants in screening, enrollment, and study visits + Experience assembling study sample collection supplies, intake biological samples, adhering to schedules, per protocol + Blood borne pathogen training and experience with blood sample handling + Experience with ultracold freezers, dry ice, and liquid nitrogen + Experience with database entry and sample tracking, biorepositories + Must be proficient in using Word, Excel, Outlook, Teams, Zoom, and REDCap + Must communicate fluently and clearly in English **DESIRED QUALIFICATIONS** + Organized, detailed oriented, excellent communicator and experienced in working in teams: + Communicating with study participants to arrange sample collection and form completion per protocol + Communicating with local providers, clinics, and laboratories to arrange sample collection, processing, and shipping of samples per protocol + Communicating with biorepository team + Communicating with a team of coordinators to accomplish study goals under oversight of senior coordinators + Strong computer skills and competency with Microsoft Office software. + Prepare common reagents + Work with other staff to ensure the lab is runs smoothly, manage restocking of study supplies and laboratory study inventory **_Other (5%)_** + May assist in performing laboratory assays + Provide input into and occasionally lead in designing or implementing new assays, experiments, or data analysis for the lab and other collaborative projects + Work with students and fellows as needed to advance research projects + Conduct laboratory tasks as assigned/needed **MINIMUM REQUIREMENTS** + Bachelor's degree in a related field and two years of experience in human studies.