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

We are looking for a Clinical Research Coordinator who is passionate about addressing health disparities, as well as has a familiarity with chronic disease management and clinical trials. The ideal candidate will function as a member of a multidisciplinary research team. Experience working in care settings serving low-income, racially ethnically diverse, and lower health literacy patient populations is desired. This role requires a high level of comfort and skill with communicating with a diverse range of stakeholders in the public health setting. This role will perform independently or with general direction at the fully operational journey level of the series to execute, manage, and coordinate research protocols, as directed by the Project Manager, Project Coordinator, and/or Principal Investigators (PI); may coordinate the data collection and operations of several concurrent clinical research studies under the guidelines of research protocols, UCSF and regulating agency policies. 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, depending on their size and complexity; act as intermediary between services and departments while overseeing data management; manage and report on study results; create, clean, update, and manage databases and comprehensive datasets and reports; coordinate staff work schedules, assist with training of Assistant CRCs, and assist with oversight of other research staff; manage Investigator's protocols in the IRB/Institutional Review Board 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; and perform other duties as assigned. Other responsibilities include supporting the stakeholder engagement, including supporting participating sites to recruit, orient, and onboard patients, community advisors, as well as professional stakeholder advisors. Additional activities may include but not be limited to developing and implementing inclusive and patient-centered engagement strategies and liaise among clinics, hospitals, and community-based organizations in the San Francisco Bay area. This position will be hybrid and the incumbent might need to travel to various clinic sites in-person across the Bay Area. The final salary and offer components are subject to additional approvals based on UC policy. Your placement within the salary range is dependent on a number of factors including your work experience and internal equity within this position classification at UCSF. For positions that are represented by a labor union, placement within the salary range will be guided by the rules in the collective bargaining agreement. The salary range for this position is $34.32 - $55.19 (Hourly Rate). To learn more about the benefits of working at UCSF, including total compensation, please visit: https://ucnet.universityofcalifornia.edu/compensation-and-benefits/index.html