Clinical Research Nurse - Intermediate

• Screens, recruits and consents study participants.
• Verifies eligibility, completes screening procedures, schedules and conducts study visits, collects and processes data collection, completes research related forms, completes electronic data entry and maintains study subject data.
• Instructs and counsels patients in research procedures, to include administration, monitoring, recording and analyzing data.
• Ensures compliance with all federal and local regulations.
• Monitors close-out of studies and ensures records are retained for appropriate length of time.
• Reviews goals and requirements of any new protocols; plans and designs source documentation for protocol; and coordinates study initiation.
• Coordinates and manages clinical research projects for Principal Investigator via study protocol including assessment, planning, evaluation and intervention for the well-being of study participants.
• Performs all other duties as assigned.

Education: Associates degree in Nursing is required.

• Ability to communicate and liaise with research participants, research team members, and other relevant partner/key stakeholders.
• Demonstrated ability to organize and coordinate work within schedule constraints and handle emergent requirements in a timely manner.
• Demonstrated ability to monitor important and complex projects concurrently.