Clinical Research Coordinator Nephrology

Job Overview The Clinical Research Coordinator (CRC) reports to the Clinical Research Supervisor and/or Principal Investigator and is responsible for executing, managing, and coordinating kidney disease clinical research protocols, including industry trials, biospecimen banking, pilot studies, and other research projects. The CRC operates independently with general direction and ensures compliance with UCSF and regulatory agency policies. Key Responsibilities Identify, recruit, screen, and enroll study participants. Schedule and conduct study visits, administer questionnaires, and perform study procedures. Maintain accurate research charts, binders, and electronic data entry in RedCap and OnCore. Manage data integrity, conduct quality‑control procedures, and analyze study data. Coordinate study operations, including specimen collection, processing, labeling, shipping, and storage. Assist in protocol submission, renewal, and amendment in the Committee on Human Research (CHR) online system. Ensure compliance with federal regulations (FDA, GCP, HIPAA), UCSF policies, and IRB requirements. Prepare and submit study progress reports, adverse events, and audit documentation. Collaborate with clinical staff, investigators, and external laboratories to facilitate smooth study execution. Perform other duties as assigned, including phlebotomy for certified candidates. Qualifications Required Qualifications High‑school graduation or equivalent experience and training; demonstrated ability to perform assigned duties. Excellent written and verbal communication skills, strong interpersonal skills, and attention to detail. Ability to work independently, manage multiple projects, and meet deadlines in a fast‑paced environment. Preferred Qualifications Proficiency with the CHR online IRB system. Experience with electronic medical records and data management platforms (RedCap, OnCore, Access, SPSS, etc.). Phlebotomy certification. Knowledge of UCSF policies on reimbursement, HIPAA, confidentiality, and patient safety. Understanding of study logistics such as specimen handling, shipping, and packaging of infectious substances. Equal Employment Opportunity The University of California is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected status under state or federal law. Salary Information Final salary and offer components are subject to UC policy approvals and depend on experience and internal equity. For further details on compensation and benefits, please refer to the UC compensation website. #J-18808-Ljbffr UCSF Health