Clinical Research Coordinator I

The Clinical Research Coordinator I provides support to the faculty of the Section of Hematology/Oncology within the Biological Sciences Division, coordinating multiple research trials types, and ensuring Standard Operating Procedures are implemented and documented in accordance to study sponsor, primary investigator, and regulatory agency specifications.

Requirements

• Coordinates all aspects of conducting clinical trials
• Maintains accurate and complete documentation of signed informed consent, relevant IRB approvals, source documentation, Case Report Forms (CRFs), drug dispensing logs, and study related communication
• Ensures Standard Operating Procedures (SOP) are implemented and documented in accordance to study sponsor, primary investigator, and regulatory agency specifications

Benefits

• Health insurance
• Retirement plan
• Paid time off