Clinical Research Coordinator

UCSF•San Francisco, CA

14d

About The Position

The 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 Supervisor, Associate Project Director, 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. The Clinical Research Coordinator will independently execute, manage, and coordinate multiple clinical research protocols within the MACS/WIHS Combined Cohort Study (MWCCS) - a collaborative, multi-center, longitudinal study designed to comprehensively investigate the impact of chronic health conditions that affect people with HIV. CRC duties may include, but will not be limited to recruiting and screening new enrollees, supporting the management and coordinating the tasks of multiple concurrent clinical research studies; act as intermediary between services and departments while overseeing data and specimen collection; clean and update, databases and comprehensive datasets and reports; coordinate staff work schedules, assist with training of new CRCs; may assist with management of Investigator’s protocols in the Investigational Review Board online system, as well as renewals and modifications of protocol applications and the implementation of new studies; 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.

Requirements

Fully operational journey level of the series.
Ability to execute, manage, and coordinate research protocols.
Ability to coordinate data collection and operations of concurrent clinical research studies.
Ability to recruit and screen new enrollees.
Ability to act as intermediary between services and departments.
Ability to oversee data and specimen collection.
Ability to clean and update databases and comprehensive datasets and reports.
Ability to coordinate staff work schedules.
Ability to assist with training of new CRCs.
Ability to assist with management of Investigator’s protocols in the Investigational Review Board online system.
Ability to manage renewals and modifications of protocol applications.
Ability to implement new studies.
Ability to assure compliance with all relevant regulatory agencies.
Ability to oversee study data integrity.
Ability to implement and maintain periodic quality control procedures.
Ability to interface with departments to obtain UCSF approval prior to study initiation.
Ability to maintain all regulatory documents.
Ability to report study progress to investigators.
Ability to participate in internal and external audits or reviews of study protocols.

Responsibilities

Execute, manage, and coordinate research protocols.
Coordinate data collection and operations of concurrent clinical research studies.
Recruit and screen new enrollees.
Act as intermediary between services and departments while overseeing data and specimen collection.
Clean and update databases and comprehensive datasets and reports.
Coordinate staff work schedules.
Assist with training of new CRCs.
Assist with management of Investigator’s protocols in the Investigational Review Board online system, as well as renewals and modifications of protocol applications and the implementation of new studies.
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 internal and external audits or reviews of study protocols.
Perform other duties as assigned.