Clinical Research Coordinator II

RESPONSIBILITIES:

• Responsible for enlisting, maintaining, and assuring protocol compliance for all patients on clinical trials.


• Ensures site research quality via Standard Operating Procedures (SOP), principles of Good Clinical Practice (GCP) and applicable federal, state, and local regulations.


• Coordinates patient care in compliance with protocol requirements.

• Responsible for accurate and timely data collection, documentation, entry, and reporting.


• Schedules and participates in monitoring and auditing activities.


• Communicates with physician regarding study requirements, need for does modification, and adverse event reporting.

QUALIFICATIONS:

• RN with Associates Degree, Bachelor's degree preferred.


• 3+ years of oncology clinical research nursing experience.


• Current BLCS or ACLS certification with SoCRA or ACRP certification preferred.

Local candidates only.