Clinical Research Coordinator - Early Phase Program | University of California San Francisco - Military Veterans

The Early Phase program has a multi-disciplinary team that works closely with patients, providing the resources and close cooperation of many specialists with deep expertise in diagnosing and treating early and late- stage cancer. Our physician-scientists are also researching and developing new and effective treatments for cancer, including clinical trials. The Early Phase program is seeking a Clinical Research Coordinator with an interest in investigational drugs to have oversight over multiple clinical research projects and support our growing program. The Clinical Research Coordinator (CRC) will independently, or with general direction, execute, manage, and coordinate clinical research protocols, as directed by the Clinical Research Manager, Principal Investigator (PI), and/or the Associate Director of Clinical Research Programs for the Early Phase program. The CRC will coordinate the administrative, data, and patient scheduling operations of several concurrent clinical research studies under the guidelines of research protocols and regulatory policies. The CRC will assist in the care of early and late-stage cancer patients while they participate in phase 1 and phase 2 clinical trials. In the role, the CRC will attend clinic appointments, follow test results, and assist in ordering appropriate study-related procedures/tests. The CRC will have the opportunity to learn certain aspects of oncology including but not limited to prevention, early detection, treatment/medication management, and end of life care for cancer patients. The CRC's duties may include, but will not be limited to, supporting the management and coordinating the tasks of single or multiple clinical research studies. This involves coordinating study required procedures and treatments for study patients; managing and updating databases to insure data integrity; acting as intermediary between sponsors, research staff, and various UCSF departments; assuring compliance with all relevant regulatory agencies; assisting Clinical Research Manager, Associate Director of Clinical Research Programs and/or PI with research tasks; maintaining relevant regulatory documents in partnership with the Regulatory department; reporting study progress to investigators; participating in any internal and external audits or reviews of study protocols; and performing other duties as assigned. Note: This position requires a physical/health screening. The final salary and offer components are subject to additional approvals based on UC policy. To see the salary range for this position (we recommend that you make a note of the job code and use that to look up): TCS Non-Academic Titles Search (https://tcs.ucop.edu/non-academic-titles) Please note: An offer will take into consideration the experience of the final candidate AND the current salary level of individuals working at UCSF in a similar role. For roles covered by a bargaining unit agreement, there will be specific rules about where a new hire would be placed on the range. To learn more about the benefits of working at UCSF, including total compensation, please visit: https://ucnet.universityofcalifornia.edu/compensation-and-benefits/index.html