Responsibilities
The Clinical Research Coordinator for the Norton Clinical Research Institute (NCRI) 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:
Desired:
The Clinical Research Coordinator for the Norton Clinical Research Institute (NCRI) 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
- Associate Degree
Desired:
- One year in Clinical Research
- Certified Clinical Research Coordinator
- Certified Clinical Research Professional