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PTSD/TBI Staff Research Associate
University of California, San Diego
This position will remain open until a successful candidate has been identified. UCSD Layoff from Career Appointment: Apply by 08/27/20 for consideration with preference for rehire. All layoff applicants should contact their Employment Advisor. Special Selection Applicants: Apply by 09/08/20. Eligible Special Selection clients should contact their Disability Counselor for assistance. DESCRIPTIONUCSD Department of Psychiatry is one of the most innovative and productive academic departments in the country, offering challenging career opportunities in the diverse areas of advanced educational programs, cutting-edge research, and state-of-the-art clinical services. The department is committed to offering a dynamic learning environment and growing opportunities to its talented and dedicated employees. Under the supervision of the Principal Investigator, the individual will work as a Staff Research Associate. Duties include assisting PI and Study Coordinator with day-to-day affairs of study coordination for protocols and administrative tasks associated with protocols at all levels of activity. Under close technical supervision, interact with PIs, Clinical Coordinator, Collaborating Scientists, pre- and post-doctoral fellows in implementing clinical protocols through regulatory approved processes, participant accrual and coordination of study activities. Track patient data in MS Excel and/or other databases. In addition, the incumbent will be trained and will assist in collection and processing of (1) EMG/PPG testing, computerized neurocognitive assessments and psychosocial scale data Under the supervision of Principal Investigator (PI), and the Clinical Research Manager, establish and maintain direct communication with PI and Co-Investigators to identify patients appropriate for multiple research studies. Consult with Clinical Research Manager on matters of recruitment and eligibility. Perform standard repetitive procedures of limited variety which include scheduling, preparing, and conducting research visits with study patients. Educate patients and families regarding study treatment, including the expected benefits and side effects of study participation. Compile and enter data and provide reports as requested by Clinical Research Manager. Assist with the preparation of applications and consent documents for submission to UCSD Human Research Protection Program (HRPP), the San Diego VA, and other subcommittees and regulatory agencies. Assist with the collection of appropriate biological specimens as required by active clinical trial protocols. Other duties as assigned by PI or Clinical Research Manager. MINIMUM QUALIFICATIONS
PREFERRED QUALIFICATIONS
SPECIAL CONDITIONS
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