Under limited supervision, the Clinical Research Coordinator I (CRC) coordinates patient care in compliance with local, state and federal guidelines and regulations through IRB approved protocol requirements
Job Summary
Under limited supervision, the Clinical Research Coordinator I (CRC) coordinates patient care in compliance with local, state and federal guidelines and regulations through IRB approved protocol requirements.
The CRC collaborates with the investigators, research staff and other departmental stakeholders to conduct clinical trial coordination per protocol.
If you would like to be part of a growing family focused on supporting clinical excellence, teamwork and innovation, we urge you to apply now!
Matching Summary
Under limited supervision, the Clinical Research Coordinator I (CRC) coordinates patient care in compliance with local, state and federal guidelines and regulations through IRB approved protocol requirements.
Skills & Requirements
Must-have
patient care compliance
IRB approved protocol requirements
clinical trial research
clear documentation
adverse event reporting
Nice-to-have
collaborative team environment
support clinical excellence
focus on innovation
Key Requirements
Technical Diploma or Degree/certification in biology, public health, pharmacy, or health related field
3 years of experience in clinical research or as a clinical trial coordinator
Proficient with computer navigation, electronic data systems, EMR, Excel, Word, PowerPoint