Clinical Research Coordinator Assistant

UCSF•San Francisco, CA

11d

About The Position

The Assistant 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 Team 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 single or multiple clinical research studies, depending on their size and complexity; act as intermediary between services and departments while overseeing data and specimen management (including collection and processing of human biospecimens: blood, urine, nasal swab); manage and report on study results; enter, clean and update databases and reports; coordinate team work schedules, assist with training of additional Assistant CRCs, and assist 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 submissions 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; 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.

Requirements

Perform independently or with general direction at the fully operational journey level of the series.

Responsibilities

Execute, manage, and coordinate research protocols.
Coordinate data collection and operations of clinical research studies.
Act as intermediary between services and departments.
Oversee data and specimen management (including collection and processing of human biospecimens: blood, urine, nasal swab).
Manage and report on study results.
Enter, clean and update databases and reports.
Coordinate team work schedules.
Assist with training of additional Assistant CRCs.
Assist PI with oversight of other research staff.
Manage Investigator’s protocols in the Committee on Human Research online system.
Manage renewals and modifications of protocol applications.
Manage the implementation of new studies.
Participate in the review and writing of submissions 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.
Maintain all regulatory documents.
Report study progress to investigators.
Participate in internal and external audits or reviews of study protocols.
Perform other duties as assigned.