The Clinical Research Coordinator I coordinates patient care in compliance with local, state and federal guidelines through IRB approved protocol requirements
Job Summary
The Clinical Research Coordinator I coordinates patient care in compliance with local, state and federal guidelines through IRB approved protocol requirements.
The role requires utilizing developing knowledge of clinical trial research to work collaboratively with individuals associated with the care and treatment of the patient.
Through clear documentation, the CRC will define any changes in condition, adverse events, concomitant medication use, protocol compliance, and response to study intervention.
Matching Summary
The Clinical Research Coordinator I coordinates patient care in compliance with local, state and federal guidelines through IRB approved protocol requirements.
Skills & Requirements
Must-have
IRB approved protocol requirements
Electronic medical records navigation
Adverse event documentation
Protocol compliance evaluation
Nice-to-have
Cardiovascular clinical experience preferred
Collaborative team environment
Opportunities for knowledge building
Key Requirements
3 years of experience in clinical research
Technical Diploma or Degree in biology or health field