Description

Summary

Assist in Section's clinical studies program. Requires Knowledge of the clinical research programs. Must be people oriented and willing to learn. Expected to work with section's faculty members and fellows in an academic medical center setting. Coordinate research projects, clinical trials, and perform duties as required by the protocol. Responsible for recruiting, screening & enrolling patients in study protocols.

Required Knowledge, Skills, and Abilities

• Proficient in data collection and entry, tabulation and CRF formatting

• Excellent written, verbal communication, interpersonal and organizational skills

• Team player, dependable, focused and takes initiative

• Proficient in Microsoft Office Applications, Windows, EMR, EPIC. EDC, IVRS, In Form

Required Education and/or Experience

• RN with a current LA license

• Minimum of five years in clinical research