Clinical Research Nurse, Enrollment

Tasks

• Attend site initiation meetings
• Collect source documents
• Complete case report forms
• Conduct clinical studies
• Dispose of waste per standards
• Ensure IRB approval
• Enter data in sponsor systems
• Execute protocol procedures
• Maintain IP accountability logs
• Maintain study compliance requirements
• Perform ECGs
• Perform informed consent
• Perform patient follow up calls
• Perform vital signs and pregnancy tests
• Provide patient medical care
• Record patient data per protocol
• Report protocol noncompliance
• Screen patients
• Update patient files and notes

Perks/Benefits

• N/A

Skills/Tech-stack

Case Report Forms | Data entry | Document verification | ECG | EDC | FDA Regulations | GCP | ICH Guidelines | IP accountability | IRB compliance | Informed consent | Patient safety | Pregnancy tests | Source document verification | Vital signs