The Clinical Research Education Analyst (Trainer 3) reports to the Director of the CTSC Clinical Trials Office, and will coordnate and maintain ongoing education programs and outreach related to the conduct of clinical trials. This position also shares educational responsibilities with the UC Davis IRB Training program.
Several years of experience in a clinical research position required; bachelor's degree in health education, public health, or business is desired.
Experience as a clinical research coordinator is strongly preferred.
Experience conceptualizing, developing, writing, editing, proofreading, and implementing print, course materials, training programs, and various other documents.
Experience conducting training, organizing and presenting to large and small groups including coordinating all required logistical details.
Analytical skills to identify and implement specific project and process improvement strategies.
Experience working with relational databases for information organization, exchange, storage, and retrieval of human subjects records.
Working knowledge of federal and state regulations, GCP guidelines, HIPAA, institutional policies, and SOPs for conduct of human subjects' research in an academic environment.
Experience in the UC Davis clinical research environment is desirable.
Must be able to travel to meetings as necessary for CTSC and IRB associated business and projects.
THIS POSITION MAY BE SUBJECT TO A CRIMINAL BACKGROUND INVESTIGATION, DRUG SCREEN, LIVE SCAN FINGERPRINTING, MEDICAL EVALUATION CLEARANCE, AND FUNCTIONAL CAPACITY ASSESSMENT
To view full job description and submit an on-line application visit UC Davis Career Opportunities at: