Clinical Research Coordinator

UCSF•San Francisco, CA

26d

About The Position

UCSF's Office for Collaborative Research (OCR) is seeking a highly motivated Clinical Research Coordinator (CRC) to join our cross-functional team in a full-time capacity. The ideal candidate will play a critical role in clinical and clinical-translational projects, acting as a link between the clinicians, research teams, study participants, and regulatory authorities. The chosen candidate’s responsibilities will encompass various aspects of the research process, from study initiation to completion. The CRC’s scope of duties encompasses, but will not be limited to, supporting the management and coordination of various clinical and clinical-translational projects, with the level of involvement varying based on the projects’ scale and intricacy. These projects may include, but are not limited to, biospecimen acquisition, chart review, interventional studies, and other research modalities. Examples of biospecimen pipelines that the candidate will be involved in can include, but are not limited to, obtaining biospecimens from cancer, autoimmune, neurological, cardiovascular, and other conditions. The candidate must demonstrate adaptability and proficiency in managing a diverse array of study types and methodologies.

Requirements

Highly motivated
Ability to act as a link between clinicians, research teams, study participants, and regulatory authorities
Adaptability and proficiency in managing a diverse array of study types and methodologies

Responsibilities

Acting as an 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
Manage OCR and 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 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
Perform other duties as assigned