Role OverviewThe Clinical Research Nurse Coordinator II will serve as primary coordinator for clinical research studies, providing quality care to participants and their families within the area of clinical specialty. The role involves managing the life cycle of the clinical trial from study start-up through trial maintenance to study closure, and performing the informed consent process following Good Clinical Practice (GCP).
What You Will Do
The successful candidate will conduct all study activities in accordance with the protocol, Institutional Review Board (IRB) regulations, and Good Clinical Practice (GCP). They will also manage participant care, including recruitment, screening, scheduling, consenting, conducting visits, and collecting various assessments such as adverse event (AE) information or questionnaires.
Why It Might Be a Fit
The ideal candidate will have a strong understanding of clinical research, protocol, and clinical trial management, with excellent problem-solving, critical thinking, teamwork, organizational skills, leadership, communication, flexibility, and emotional intelligence.
Requirements
- Bachelor's degree in a related field
- Three (3) years of related experience
- Currently licensed as a Registered Nurse (RN) by the Alabama Board of Nursing
- Knowledge of Oncology, clinical research, protocol, and clinical trial management
Benefits
- Annual Salary Range: $60,835 - $98,855
- Paid holidays
- Vacation time
- Sick leave
- Health insurance
- Retirement plan
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