Description

Summary

The primary responsibility of the Clinical Research Coordinator II is to coordinate and conduct the day-to-day operation of clinical studies and clinical trials. The Clinical Research Coordinator II assists the investigator team in developing study protocols and manuals of procedures. The Clinical Research Coordinator II screens, enrolls, and follows study participants, conducts data collection and entry, and performs tests according to study protocols. The Clinical Research Coordinator II is also responsible for keeping all data and source documentation, adverse event reporting, and IRB regulatory files.

Required Knowledge, Skills, and Abilities

• Must be able to interact well with patients and the general public
• Ability to acquire and maintain all required CITI training certificates

• Ability to acquire and maintain credentialing at all required institutions

• Ability to maintain confidentiality in all work performed

• Proficient in various software programs (including database management [e.g. Access], presentation packages [e.g. PowerPoint], spreadsheets [e.g. Excel], and advanced word processing [e.g. Word]).

Required Education and/or Experience

• Bachelor's Degree or RN with current state licensure at the time of hire and one (1) year of related work experience
OR

• LPN with current state licensure at the time of hire and four (4) years of related work experience

OR

• Master's Degree in a related field

Preferred Qualifications

• Knowledge of IRB submission process and requirements
• Knowledge of good clinical practices as set forth by federal regulations