A company is looking for a Clinical Research Coordinator, RN.
Key Responsibilities
Communicate with Study Sponsors, CROs, and staff regarding protocol status and concerns
Monitor study conduct for compliance with protocols, SOP, and Good Clinical Practice
Assist with patient screening, eligibility determination, and the informed consent process
Required Qualifications and Education
Associate's degree in Nursing and RN license in California
2 years of clinical research experience with a basic understanding of oncology Phase 1 trials
Proficient in Microsoft Office Suite and clinical trial management software
Knowledge of Good Clinical Practice and regulatory requirements
Experience in an oncology setting is preferred
Clinical Research Coordinator • Springfield, Missouri, United States