Clinical Research Coordinator
About The Position
In the UCSF Memory and Aging Center, the ALBA Language Neurobiology laboratory is directed by the PI and the Tee Lab is led by Dr. Boon Lead Tee. The ALBA lab study how language is organized into brain networks across the lifespan. ALBA group research how language skills and brain regions are impacted by neurological conditions and how they reorganize in response. The Tee Lab focuses on scientific research that encourage equal representation from diverse populations worldwide in cognitive and dementia research, which would greatly enhance our neuroscientific understanding to brain aging and neurodegenerative diseases. The Tee Lab aims to address current calls for culturally and linguistically appropriate cognitive assessment tests, stimulate the development of novel tests for syndromic differentiation in different languages, and enhance our understanding to various neural mechanism by promoting language diversity in cognitive research. The Tee lab has collaboration with scientists and researchers from Taiwan, Hong Kong, Korea, India and Turkey, aiming to delineate the neural mechanism of bilingualism and dementia syndromes through cross-linguistic perspectives, promote language diversity in cognitive research and offer equitable care for speakers of different languages. This position will be a joint position between the ALBA and Tee lab. Under the supervision of Principal Investigators (PIs), the incumbent will perform entry-level duties related to the support and coordination of clinical studies of participants with language difficulties enrolled within the UCSF Memory and Aging Center and may receive training and development to prepare and advance for journey-level work at the next level within the series.
Requirements
- Entry-level duties related to the support and coordination of clinical studies of participants with language difficulties
- May receive training and development to prepare and advance for journey-level work at the next level within the series
Responsibilities
- May be responsible for the coordination of one or more single or multi-site, active or follow-up trials
- Help prepare protocols for study initiation
- Help design flow sheets, data forms and source documents
- 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
- Perform other duties as assigned
Benefits
- Total compensation
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What This Job Offers
Career Level
Entry Level
Education Level
No Education Listed
