Senior Clinical Research Coordinator
University of California, San Francisco · San Francisco
The Senior Clinical Research Coordinator (CRC) is an experienced professional who independently coordinates and is accountable for the overall administration of one or more clinical and implementation studies, requiring advanced-level knowledge and skills. The Senior CRC will support two studies, a domestic industry collaboration around diagnostic assay development, and a drug-resistant tuberculosis laboratory-based study in South Africa, as well as other studies as assigned.
The Senior CRC will be responsible for managing study communications across multiple stakeholders, ensuring timely implementation of research activities, overseeing operational and administrative functions, and managing other team members, as needed. Travel will be required to study sites, and to international study locations (South Africa, and potentially other sites). The position requires strong scientific writing skills, program management skills, flexibility and adaptability to move between studies in international and domestic settings, and a willingness to complete tasks regardless of level of responsibility. Knowledge and experience working on domestic and/or international research studies focused on TB, HIV and COVID-19 is highly desired.
Under the direction of Project Director’s/Principal Investigator’s, the senior CRC will engage in the following activities:
Develop plans to ensure research commitments are met, and ensure timely implementation of research activities
Provide high-level communications and facilitation support to ensure collaboration among multiple study stakeholders
Write, develop, and manage a range of scientific publications, including reports, articles, and other written materials, from initial concept through final production, ensuring content is accurate, well-organized, and aligned with academic standards.
Manage other team members, deliverables, timelines, and dissemination of reports and publications
Ensure committee on human research approval and compliance
Manage contract negotiations with study partners and provide contract oversight
Provide support to manage study databases
Conduct statistical analyses and database management fundamental to project monitoring and/or summary
Support principal investigators with budget monitoring and procurement of study supplies, as needed
Support principal investigators to troubleshoot any issues that arise within the pragmatic trial or the implementation research study
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