CLINICAL RESEARCH NURSE COORDINATOR I

General Responsibilities

• Serve as coordinator for clinical research studies and provides support to other study team members for research trials, studies, and projects within the confines of the study protocols as directed.
• Support protocol screening and study participant eligibility determination, working with more senior study team members to ensure compliance.
• Conduct all study activities in accordance with the protocol, Institutional Review Board (IRB) regulations, and Good Clinical Practice (GCP).
• May provide quality care to participants and their families within the area of clinical specialty.
• To assist with the life cycle of the study from start-up through maintenance to closure.
• Care coordination including recruitment, screening, scheduling, consenting, conducting visits, and collecting various assessments such as adverse event (AE) information or questionnaires.
• Perform the informed consent process following GCP.
• Act as a liaison among the clinical and research staff, departments, ancillary services and the study sponsor to ensure protocol compliance throughout the study.

Requirements

• Bachelor's degree in a related field required.
• Work experience may substitute for education requirement.
• Currently licensed or eligible to be licensed as a Registered Nurse (RN) by the Alabama Board of Nursing required.
• Organized, detail-oriented, and compassionate RN who is proficient in phlebotomy and documentation.
• This employee will coordinate multiple clinical trials independently.

Qualifications

None specified.

Skills

Not specified.

Benefits

Not specified.

Pay

Annual Salary Range: $52,555 - $85,400

Schedule

Day/1st Shift

Organization

Neurology Chair Office

Employee Status

Regular

Shift Type

Hybrid Eligible