CLIN RSCH CRD AST

March 27, 2024
Neuro-Memory and Aging
Full Time
Req Number: 
77520BR
Under the supervision of Adam Boxer, MD, PhD and Adam Staffaroni, PhD, the Assistant Clinical Research Coordinator (ACRC) will have the opportunity to work on studies that seek to improve equitable access to care by validating digital (i.e., smartphone assessments) and blood-based biomarkers of dementia, with a focus on underrepresented groups. The ACRC will work on UCSF-based and multi-center North American studies of Alzheimer’s disease, frontotemporal dementia, and healthy aging. The ACRC will be working with both English- and Spanish-speaking participants. They will be responsible for recruitment and enrollment of participants from ongoing studies and community clinics, and they will conduct study visits. They may also be involved in cross-cultural implementation and interviewing participants about their experience. Spanish and English fluency is a requirement. The ACRC does not need to have any advanced knowledge of digital technologies and will not be asked to conduct any specimen collection (i.e., phlebotomy).

The ACRC will be responsible for the support and coordination of data collection; help prepare protocols for study initiation; data forms and source documents; may be responsible to gathering medical data regarding study participants; may apply understanding of inclusion/exclusion eligibility criteria for protocols; help recruit, enroll, register, schedule and retain study subjects; record protocol specific treatments and assure collection and shipment of samples; assist research personnel to keep patients on study schedules; complete study forms to submit to sponsors and/or appropriate agencies; collect, enter and clean data into study databases, maintaining data quality; assist with data analysis; assist with preparation of reports and tables; attend team meetings; monitor device output for the duration of the study; manage IRB submissions and modifications; may provide technical support to participants and/or study team; communicate study proceedings with team and outside collaborators; and perform other duties as assigned.

The final salary and offer components are subject to additional approvals based on UC policy.

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