Clinical Research Coordinator I

The Clinical Research Coordinator I (CRC I) is a specialized research professional working with and under the direction of the clinical Principal Investigator (PI). The job performs routine assignments related to the documentation and reporting of basic clinical studies, supports decisions that impact clinical research conducted across the University, and executes study procedures in accordance with protocol requirements.

Requirements

• Coordinate all aspects of conducting clinical trials including: screening, enrollment, subject follow-up, completion of case report forms (CRFs), and adverse event (AE) reporting.
• Maintain accurate and complete documentation of signed informed consent, relevant IRB approvals, source documentation, CRFs, drug/device accountability logs, and study-related communication.
• Perform specific protocol procedures (specimens and data management, survey/questionnaire administration, etc.) required to conduct the study and retain research subjects.
• Plan and coordinate patient schedules for study procedures, return visits, and study treatment timelines.
• Ensure Standard Operating Procedures (SOPs) are implemented and documented in accordance with study sponsor, PI, and regulatory agency requirements.

Benefits

• Health insurance
• Retirement plan
• Paid time off