CLIN RSCH CRD

May 31, 2024
Neuro-Memory and Aging
Full Time
Req Number: 
78850BR
The UCSF Dyslexia Center focuses on improving diagnosis, care, and interventions for children and adults with learning challenges. The Center is currently comprised of three research studies each led by different principal investigators. The Phenotyping Study is led by Dr. Gorno-Tempini in the Neurology Department with the aim of discovering different phenotypes of dyslexia through a curated battery of cognitive, language, neuroscience and neuroimaging studies. The Clinical Research Coordinator will coordinate information, correspondence, appointments, and meetings between study personnel, participant families, and partner schools.

The Clinical Research Coordinator will perform independently execute, manage, and coordinate research protocols, as directed by the Clinical Research Supervisor and/or Principal Investigator (PI); may coordinate the data collection and operations of several concurrent clinical research studies under the guidelines of research protocols, UCSF and regulating agency policies.

Incumbent’s duties may include, but will not be limited to supporting the management and coordinating the tasks of multiple clinical research studies; act as intermediary between services and departments while overseeing data and specimen management; manage and report on study results; create, clean, update, and manage databases and comprehensive datasets and reports; coordinate staff work schedules, assist with training of Assistant CRCs, and assist Clinical Research Supervisor and/or PI with oversight of other research staff; 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.

To see the salary range for this position (we recommend that you make a note of the job code and use that to look up): TCS Non-Academic Titles Search (https://tcs.ucop.edu/non-academic-titles)

Please note: An offer will take into consideration the experience of the final candidate AND the current salary level of individuals working at UCSF in a similar role.

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