Clinical Research Coordinator - Immunox / Immunology / Collaborative Research | University of California San Francisco - Military Veterans

The Bakar ImmunoX Initiative is an ambitious, first-in-class program at UCSF that uses social engineering, state-of-the-art technologies and infrastructure, and a unique data-sharing model to support a large community of researchers and clinicians as they seek to harness immunology to improve human health. By restructuring traditional research, we create opportunities for cross-fertilization of ideas, discoveries, and insights. UCSF's ImmunoX Office for Collaborative Research (OCR) is seeking a highly motivated and experienced 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-translational research 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-translational research 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. Responsibilities for this position include: 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; and perform 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. 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