Essential duties include: review medical records and completion of Case Report Forms (CRF's) as required by Study Protocols, assist with handling MRI data and images for Research Studies for transferring to Study Sponsors, attend research meetings and provide updates for our site regarding study status, perform data quality control and query, prepare periodic written and oral report summaries, coordinate recruitment (e.g., screen eligible patients through medical record review, create and post study recruitment material), consent and enroll human participants from clinic and hospital areas, schedule research participants to complete research activities, collect biospecimens (blood, saliva, CSF, & brain tissue) and complete tests ( MRI, biometric device) and questionnaires, coordinate shipping or transfer of samples, assist IRB documents (amendments, continual review), maintain detailed records of research activities (study protocols, records of subject enrollment and sample collection), maintain and order supplies as needed for research projects, maintain the office workspace area in a clean and safe condition, and perform other routine duties as assigned.