Clinical Research Coordinator

The Clinical Research Coordinator's duties may include, but will not be limited to, coordinating the tasks of multiple clinical research studies within the Department of Emergency Medicine; 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; train research volunteers; coordinate all 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.

This position reports to the department's Administrative Manager for operational, administrative, and financial matters, and to the Research Director for research direction and regulatory compliance.

Department Overview:

UCSF Fresno is a regional campus of UCSF located in California’s Central San Joaquin Valley and administered by the Office of the Vice Dean in Fresno. 

The UCSF Fresno Department of Emergency Medicine is a medium-to large-sized academic department, with 46 residents, three fellows, 75 faculty, 16 midlevel providers, and approximately 60 medical student rotators. Founded in 1974 at Valley Medical Center in Fresno County, the Emergency Medicine residency is one of the first EM programs in the country. 

The UCSF Fresno Emergency Medicine Department provides service and training at the affiliated locations: Community Regional Medical Center, Clovis Community Medical Center, and Kaiser Permanente Fresno. The Department’s mission is: Advancing Emergency Medicine through exceptional education, patient care, research, and collaboration.

20% Study Coordination

• Prepare all relevant Institutional Review Board (IRB) paperwork (e.g., initial review documents, study renewals/closure reports, adverse events, study modifications, etc.). Review, edit, and format all research protocols and consent documents before submitting all materials through CyberIRB.

• Obtain informed consent; review information with subjects; conduct follow-up calls; assess and advocate for patient safety throughout each protocol procedure.

• Oversee subject reimbursement; work to resolve discrepancies and issues.

• Conduct reviews of medical charts and electronic records to extract medical information and other data for use in studies.

• Implement needs assessments and recommendations for enhancements on patient coordination, data collection, data management, protocol adherence and study collaboration.

• Act as liaison between departments, stakeholders, and UCSF.

• Respond to queries from the IRB in a timely manner.

20% Data Management

• Manage database structure for each protocol; update databases to improve data analysis and management; create new databases as needed.

• Maintain data collection forms for effective data collection, entry, and analysis.

• Maintain electronic study records and regulatory study binders.

• Maintain research log in Microsoft Excel of all ongoing projects in Emergency Medicine.

• Work with study PIs to ensure compliance with clinical protocols and federal guidelines.

• Maintain records of Human Subjects Protection Training for all personnel involved in departmental research studies.

25% Staff, research associates, and volunteer training

and coordination

• Help train staff, research associates/volunteers, and others on new research protocols, research fundamentals, changes in procedures, study protocols, data collection/entry, database procedures, medical chart review and storage, and other procedures.

• Assist research director with the development and updates to a curriculum for volunteer research associates that covers clinical research fundamentals.

• Support research director with the selection, training, and utilization of volunteer research associates.

• Help research director guide research associate