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This position performs a variety of complex duties involved in a clinical research study setting in support of research initiatives; and assists the Clinical Trials Office as a whole. Duties include, but are not limited to, providing continual support to the clinical research trials to be conducted within federal, state, and local regulations. This position will also be responsible for studies assigned by PI, patient data collection and entry. Responsible for ensuring all data is handled in accordance to HIPAA and all other applicable AU regulations, policies, and procedures. Performs high quality data abstraction that is accurate and suitable for statistical analysis. Data meets the protocol specific parameters and comply with all other applicable regulations, policies and procedures.