Job Summary
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, SOPs, and Good Clinical Practice
- Assist with patient screening, eligibility determination, and informed consent process
Required Qualifications
- Associate's degree in nursing and RN license in New Jersey
- 2 years of clinical research experience, with knowledge 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
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