Coordinator, Clinical Research-Oncology Research Operations, Days 8a-430p
Norton Healthcare
Date: 12 hours ago
City: Louisville, Kentucky
Contract type: Full time
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:
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
- One year in Clinical Research
- Certified Clinical Research Professional OR Certified Clinical Research Coordinator
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