Assistant Clinical Research Coordinator
About The Position
Under the supervision and guidance of the Principal Investigator and Clinical Research Supervisor at the UCSF Memory and Aging Center, the Assistant Clinical Research Coordinator (ACRC) will serve as a liaison between research participants and other faculty/study staff members to perform entry-level duties related to the support and coordination of clinical studies in the UCSF Alzheimer’s Disease Research Center and associated projects. The ACRC will be responsible for the support and coordination of various clinical research studies, including single- and multi-site clinical trials and observational studies in the field of neurodegenerative disease. This candidate will be responsible for understanding study protocols and the associated inclusion/exclusion eligibility criteria to assist in the screening and enrollment of participants. The ACRC will coordinate the scheduling of study visit events such as neurological exams, nursing interviews, biospecimen collection, and will work to retain research participants though the end of their research participation. The ACRC may also assist in acquiring MR images, in administering cognitive assessments, and in data entry and discrepancy resolution tasks in the study databases. Additional administrative tasks may be assigned as needed to help design flow sheets, data forms, and other types of source documents.
Requirements
- Entry-level duties related to support and coordination of clinical studies.
- Understanding of study protocols and inclusion/exclusion eligibility criteria.
- Coordination of study visit scheduling.
- Participant retention efforts.
- Assistance with MR image acquisition.
- Administration of cognitive assessments.
- Data entry and discrepancy resolution.
- Assistance with administrative tasks such as designing flow sheets, data forms, and source documents.
Responsibilities
- Serve as a liaison between research participants and other faculty/study staff members.
- Perform entry-level duties related to the support and coordination of clinical studies.
- Understand study protocols and associated inclusion/exclusion eligibility criteria to assist in screening and enrollment of participants.
- Coordinate the scheduling of study visit events such as neurological exams, nursing interviews, and biospecimen collection.
- Work to retain research participants through the end of their research participation.
- Assist in acquiring MR images.
- Administer cognitive assessments.
- Perform data entry and discrepancy resolution tasks in study databases.
- Assist in designing flow sheets, data forms, and other types of source documents.
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What This Job Offers
Career Level
Entry Level
Education Level
No Education Listed
