Coordinator, Clinical Research, NCIRP Research Operations, Days

Responsibilities

The Clinical Research Coordinator (CRC) is responsible, under the direction of the principal investigator, to manage and/or execute all aspects of clinical research protocols in accordance with Standard Operating Procedures (SOPs), Norton Healthcare policy, and FDA regulations and/or GCP guidelines. The CRC functions as a liaison between patients, investigators, local clinic, sponsors, Norton Healthcare Research Office and their research management team. The CRC represents Norton Healthcare Research as assigned clinics within the community.

Qualifications

Required:

• One year in healthcare
• Bachelor Degree

Desired:

• One year in Clinical Research
• Certified Clinical Research Professional OR Certified Clinical Research Coordinator