The job functions include: Source documentation generation in study startup; Contacting patients and caregivers to schedule research visits, Tracking enrollment progress; Organizing and coordinating research visits; Run the study visit (cognitive testing, MRI, biofluids) per protocol; Biofluid collection, processing, and shipping per protocol; Maintain records of monthly/yearly progress reports, protocols and ICFs tracking and version control in shared drive, Maintain source documentation of study activities, including essential document and correspondence; Invoice study activities, Perform subject reimbursement according to study protocol and verify accuracy; Perform data entry; Performing preliminary cognitive or imaging analyses if applicable. Applicants with prior experience with federally funded clinical research, multi-site research studies, early onset neurodegenerative disease, relevant regulations for the conduct of clinical research including Title 21 Code of Federal Regulations (CFR), International Conference of Harmonization (ICH) Guidelines, etc. are preferred.