"CLINICAL RESEARCH NURSE COORDINATOR II"

Posted: 05-Dec-25

Location: Birmingham, Alabama

Type: Regular

Categories: Staff/Administrative

Internal Number: T231348

The University of Alabama at Birmingham (UAB), Med - Endocrinology, Diabetes & Metabolism, is seeking a Clinical Research Nurse Coordinator II. This position will support clinical research in the Basu Laboratory under the direction of Dr. Ananda Basu and Dr. Rita Basu.

General Responsibilities

• To serve as primary coordinator for clinical research studies and supporting more senior team members.
• To provide a lead role in protocol screening and participant eligibility determination working alongside other team members to ensure compliance. May provide oversight to junior clinical research coordinators (CRC) and clinical research nurse coordinators (CRNC) in review of study documents.
• To conduct all study activities in accordance with the protocol, Institutional Review Board (IRB) regulations, and Good Clinical Practice (GCP).
• To provide quality care to participants and their families within the area of clinical specialty.
• To coordinate the life cycle of the study from start-up through maintenance to closure.
• To manage participant care including recruitment, screening, scheduling, consenting, conducting visits, and collecting various assessments such as adverse event (AE) information or questionnaires. To perform the informed consent process following GCP.
• To act as a liaison between the clinical and research staff, departments, ancillary services and the study sponsor to ensure protocol compliance throughout the study.
• Performs other duties as assigned.

Annual Salary Range: $60,835 - $98,855

Qualifications

Bachelor's degree in a related field and three (3) years of related experience required. Work experience may substitute for education requirement. Currently licensed as a Registered Nurse (RN) by the Alabama Board of Nursing required.

Preferences

• Previous experience and knowledge of clinical research, IRB, NIH, human subject protocols, informed consent, etc., is highly preferred.