Clinical Research Coordinator
About The Position
The Clinical Research Coordinator (CRC) will join the Radiology CRC Core within the UCSF Department of Radiology and Biomedical Imaging. The Radiology CRC Core is a team of personnel that provide expertise in conducting clinical research studies, including study setup, execution, management, IRB submissions, clinical research rates, and other research-related activities. The CRC 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 Clinical Research Supervisor and/or Principal Investigator (PI). 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; coordination, recruitment and enrollment of research subjects; data collection, data entry, data transfers, and data management; act as intermediary between services and departments; assist with training of Assistant CRCs and other CRC team members, and assist Clinical Research Supervisor and/or PI with oversight of other research staff; other duties as assigned. This work may involve travel between different imaging centers at multiple UCSF campuses as well as interacting with study physicians, researchers, technologists and patients. Studies that the CRC may be involved with include both investigator-initiated and industry-initiated clinical trials. The incumbent may be assigned a variety of studies within the various clinical sections of Radiology such as Abdominal Imaging, Breast Imaging, Cardiac & Pulmonary Imaging, Interventional Radiology, Molecular Imaging & Therapeutics, Musculoskeletal, Neuroradiology, Neurointerventional Radiology, and Pediatric Radiology. The Core also collaborates on studies with investigators in other departments such as neurology, endocrinology, oncology, nuclear medicine, radiation oncology, and the UCSF HDFC Cancer Center. 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
Requirements
- HS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities; and/or equivalent experience/training
- Experience working with patients or study subjects
- Excellent verbal and written communications and presentation skills; excellent organizational skills; and excellent interpersonal skills to work effectively in a diverse team.
- Proficiency with Microsoft Word, PowerPoint, and Windows.
- Excellent analytical and problem-solving skills.
- Ability to work effectively in a fast-paced, team-based environment; project management and coordination skills; ability to prioritize tasks and meet multiple deadlines on concurrent projects.
- Ability to establish cooperative working relationships with patients, co-workers, & physicians.
- Ability to abstract data from medical records and transfer it to data collection forms or directly into databases
- Ability to work under minimal supervision.
- Strong accuracy and attention to detail
- Excellent verbal and written communications and presentation skills; excellent organizational skills; and excellent interpersonal skills to work effectively in a diverse team
- B.A. or B.S degree with a major in science or related
- Training/experience in the conduct of clinical research trials in an academic research environment
- Familiarity with UCSF processes and systems; experience and knowledge of IRB policy and procedure.
- Related lab/research experience
- Experience running clinical research studies, with a strong understanding of Institutional Review Board (IRB) protocols
- Experience with establishing/running a clinical trial
- Experience with data entry and cleaning
- Navigating study procedures, experience with consents, reviewing eligibility criteria, reporting of safety listings, entering of data and orders into medical record system, coordination and scheduling of hospital visits and follow ups with participants and study staff
Responsibilities
- supporting the management and coordinating the tasks of single or multiple clinical research studies, depending on their size and complexity
- coordination, recruitment and enrollment of research subjects
- data collection, data entry, data transfers, and data management
- act as intermediary between services and departments
- assist with training of Assistant CRCs and other CRC team members, and assist Clinical Research Supervisor and/or PI with oversight of other research staff
- other duties as assigned
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
High school or GED
Number of Employees
5,001-10,000 employees
