The Senior Clinical Research Coordinator (Sr. CRC) provides an advanced-level working knowledge and leadership of clinical trial management activities in the UC Davis Alzheimer’s Disease Center, East Bay. Under the direction of Principal Investigators and the Clinical Research Supervisor, the incumbent is responsible for daily study activities and plays a key role in the study conduct and management. The incumbent is responsible for organizing the documentation and files pertaining to studies and for coordinating activities of investigators and study participants. This position requires the use of skills to independently coordinate and follow through in overall administration and outcome of clinical studies. Incumbent will recruit and screen study participants, coordinate the clinical treatment and follow-up care as it pertains to study protocol, facilitate continued participation; abstract data from medical records and other sources; collect, submit and maintain study data and regulatory documents; develop and ensure compliance with study protocols; and participate in the planning, development and budgeting of clinical studies and oversee the day to day activities of the ADC East Bay clinical trial coordinators
Senior Clinical Research Coordinators have achieved professional certifications in Clinical Research and are expected to independently manage large complex studies. This level requires use of advanced-level knowledge and skills to independently coordinate, direct and follow through in the overall administration and outcome of one or more clinical studies. The incumbent will provide leadership for the ADC clinical research program, including guiding and mentoring clinical research coordinators, associates, and/or other support personnel.
A minimum of 3-5 years of experience as a Clinical Research Coordinator, with demonstrated increasing level of responsibility
Society for Clinical Research Associates (SOCRA) Certified Clinical Research Professional (CCRP) or Association of Clinical Research
Professional (ACRP) Certified Clinical Research Coordinator (CCRC)
Advanced knowledge of regulatory processes as well as a working knowledge of data management activities.
Advanced-level knowledge of federal, local, and institutional regulatory guidelines.
Thorough knowledge of and regulations related to FDA, state & federal guidelines, and Good Clinical Practices, for drug and device studies (clinical research involving human subjects).
Advanced level knowledge and skills to independently coordinate, direct, and follow through in the overall administration and outcome of one or more clinical studies.
Advanced-level knowledge of basic anatomy, medical terminology, and ability to interpret physicians' notes, medical records, laboratory and scan results.
Advanced analytical skills to evaluate information, practices, and procedures, formulate logical and objective conclusions and make recommendations for effective solutions.
Administrative skills and ability to exercise good judgment, initiative, and resourcefulness in making decisions.
Experience and working knowledge of but not limited to: scheduling and medical record systems, Microsoft Word, Excel, Access and etc.
This position may be subject to a criminal background investigation, drug screen, Live Scan fingerprinting, medical evaluation clearance, and functional capacity assessment.
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