Assistant CRC

UCSF•San Francisco, CA

5d•$32 - $32•Onsite

About The Position

The Assistant Clinical Research Coordinator will assist the PI with clinical research coordination of the following studies: (1) a pediatric headache study sponsored by PCORI. UCSF is identified as an enrolling site. Under the PI and Clinical Research Manager; the incumbent may coordinate the data collection and operations of this trial (REACH) Responding with Evidence and Access for Childhood and Headaches under the guidelines of the Code of Federal Regulations, Good Clinical Practice, and UCSF policies. (2) a pediatric headache study sponsored by Pfizer. Under the PI and Clinical Research Manager; the incumbent may coordinate the data collection and operations of this study Empowering Children and Adolescents Undergoing Needle-based Procedures for Headache Treatment through Implementation of a “Headache Procedure Comfort Menu”: a Novel Clinical Tool under the guidelines of the Code of Federal Regulations, Good Clinical Practice, and UCSF policies. The 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 of varied size and complexity; help in research administration; assist with patient recruitment; help manage patient study source documents; perform data entry to study Case Report Form databases; collect, process and ship study specimens in accordance with study protocols; assist the PI with intermediary services and departments while overseeing data and specimen coordination; report study progress to the PI in regular team meetings; update spreadsheets tracking recruitment efforts; help coordinate subcontracts through collaborative effort with PI; assist with management of all Regulatory aspects of Investigator’s protocols in IRIS, the Committee on Human Research online system, including renewals and modifications of study protocols and the implementation of new studies; ensure study data integrity; assist with implementation of quality control procedures; participate in any internal and external audits or reviews of study protocols; and perform other duties as assigned as appropriate.

Requirements

Under the PI and Clinical Research Manager
Coordinate the data collection and operations of this trial (REACH) Responding with Evidence and Access for Childhood and Headaches
Coordinate the data collection and operations of this study Empowering Children and Adolescents Undergoing Needle-based Procedures for Headache Treatment through Implementation of a “Headache Procedure Comfort Menu”: a Novel Clinical Tool
Guidelines of the Code of Federal Regulations
Good Clinical Practice
UCSF policies

Responsibilities

Support the management and coordination of single or multiple clinical research studies of varied size and complexity.
Assist in research administration.
Assist with patient recruitment.
Help manage patient study source documents.
Perform data entry to study Case Report Form databases.
Collect, process, and ship study specimens in accordance with study protocols.
Assist the PI with intermediary services and departments while overseeing data and specimen coordination.
Report study progress to the PI in regular team meetings.
Update spreadsheets tracking recruitment efforts.
Help coordinate subcontracts through collaborative effort with PI.
Assist with management of all Regulatory aspects of Investigator’s protocols in IRIS, the Committee on Human Research online system, including renewals and modifications of study protocols and the implementation of new studies.
Ensure study data integrity.
Assist with implementation of quality control procedures.
Participate in any internal and external audits or reviews of study protocols.
Perform other duties as assigned as appropriate.