CLIN RSCH CRD

CLIN RSCH CRD

University of California San Francisco - 4.1 Oakland, CA Job Details Full-time 3 hours ago Qualifications Project team coordination Clinical study protocols and reports Scientific research Mid-level Databases Data quality management Clinical research compliance Scientific protocols Quality control Regulatory submissions Research regulatory compliance IRB compliance Regulatory audits Internal audits Full Job Description This is a limited appointment that will end when the project concludes or when the incumbent reaches 1,000 hours worked, whichever occurs first. 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. This role operates under the guidance of the Clinical Research Supervisor and/or Principal Investigator (PI) within the Department of Pediatrics and may support multiple concurrent clinical research studies in accordance with research protocols, UCSF policies, and regulatory agency requirements. Responsibilities include, but are not limited to, managing and coordinating activities for one or more clinical research studies, depending on size and complexity; serving as a liaison between departments and services; and overseeing data and specimen management. The incumbent will create, maintain, and analyze databases and comprehensive datasets; manage and report study results; and support scheduling and coordination of study team activities. Additional duties include managing investigator protocols within the Committee on Human Research (CHR) system, including submissions, renewals, and modifications; supporting the initiation of new studies; and assisting in the preparation and review of study protocols to ensure Institutional Review Board (IRB) approval and compliance with university and regulatory standards. The role also ensures adherence to all applicable regulatory requirements, maintains study documentation, monitors data integrity, and implements quality control procedures. The Clinical Research Coordinator will interface with internal departments to obtain required approvals, report study progress to investigators, and participate in internal and external audits. Other duties may be assigned as needed.