October 29, 2025
Neuro-Memory and Aging
Full Time
Req Number:
86668BR
The Clinical Research Coordinator will perform independently or with general direction at the fully operational journey level of the series to execute, manage, and coordinate research protocols, as directed by the Clinical Research Supervisor and/or Principal Investigator (PI).
As a member of Dr. Gil Rabinovici’s Lab within the Memory and Aging Center, this position serves to be a liaison between research participants, collaborators, and staff members to carry out study functions under the direction of the Principal Investigator(s). Incumbent’s duties may include but will not be limited to supporting the management and coordinating the tasks of single or multiple clinical research studies, depending on their size and complexity. This position will take the lead in coordinating a wide range of staff member's schedules to enroll participants, conduct neuropsychological tests, run MRI scans, collect specimen samples, track collection, present data requests, organize periodic operational meetings, collaborate with sub-projects, and lead the training of Assistant CRCs. In addition, there will be in depth knowledge of daily functions and the ability to answer study inquiries (in-person, phone, email, etc) as they arise. The studies will enroll patients with neurodegenerative disease such as Alzheimer’s disease which causes cognitive and behavioral problems. Therefore, experience working with elderly populations and people with neurobehavioral symptoms, such as neurological or psychiatric patients, is strongly preferred. A minimum 2-year commitment is required.
With time and experience, the incumbent may expand their knowledge base and may evolve to manage Investigator’s protocols in the Committee on Human Research online system, as well as renewals and modifications of protocol applications and the implementation of new studies; participate in the review and writing of protocols to ensure institutional review board approval within University compliance; help assure compliance with all relevant regulatory agencies; oversee study data integrity; implement and maintain periodic quality control procedures; interface with departments to obtain UCSF approval prior to study initiation; maintain all regulatory documents; report study progress to investigators; participate in any internal and external audits or reviews of study protocols; and perform other duties as assigned.
As a member of Dr. Gil Rabinovici’s Lab within the Memory and Aging Center, this position serves to be a liaison between research participants, collaborators, and staff members to carry out study functions under the direction of the Principal Investigator(s). Incumbent’s duties may include but will not be limited to supporting the management and coordinating the tasks of single or multiple clinical research studies, depending on their size and complexity. This position will take the lead in coordinating a wide range of staff member's schedules to enroll participants, conduct neuropsychological tests, run MRI scans, collect specimen samples, track collection, present data requests, organize periodic operational meetings, collaborate with sub-projects, and lead the training of Assistant CRCs. In addition, there will be in depth knowledge of daily functions and the ability to answer study inquiries (in-person, phone, email, etc) as they arise. The studies will enroll patients with neurodegenerative disease such as Alzheimer’s disease which causes cognitive and behavioral problems. Therefore, experience working with elderly populations and people with neurobehavioral symptoms, such as neurological or psychiatric patients, is strongly preferred. A minimum 2-year commitment is required.
With time and experience, the incumbent may expand their knowledge base and may evolve to manage Investigator’s protocols in the Committee on Human Research online system, as well as renewals and modifications of protocol applications and the implementation of new studies; participate in the review and writing of protocols to ensure institutional review board approval within University compliance; help assure compliance with all relevant regulatory agencies; oversee study data integrity; implement and maintain periodic quality control procedures; interface with departments to obtain UCSF approval prior to study initiation; maintain all regulatory documents; report study progress to investigators; participate in any internal and external audits or reviews of study protocols; and perform other duties as assigned.
The final salary and offer components are subject to additional approvals based on UC policy.
Your placement within the salary range is dependent on a number of factors including your work experience and internal equity within this position classification at UCSF. For positions that are represented by a labor union, placement within the salary range will be guided by the rules in the collective bargaining agreement.
The salary range for this position is $34.32 - $55.19 (Hourly Rate).
To learn more about the benefits of working at UCSF, including total compensation, please visit: https://ucnet.universityofcalifornia.edu/compensation-and-benefits/index.html
