CLINICAL RESEARCH NURSE COORDINATOR I

UAB group; Birmingham (AL); On-site; USD 53,000 - 85,000; Full time

Job summary

The University of Alabama at Birmingham (UAB) Department of Ped - Hematology/Oncology is seeking a Clinical Research Nurse Coordinator I to support pediatric oncology trials. This role ensures protocol compliance, coordinates patient care for research participation, and collects data and specimens for regulatory reporting.

The coordinator will liaise with patients, providers, sponsors, and the research team, supporting GCP/IRB requirements and audit readiness.

Qualifications

• Bachelor's degree in a related field required.
• Currently licensed or eligible to be licensed as a Registered Nurse (RN) by the Alabama Board of Nursing.
• Onsite nursing role with day shift responsibilities.

Responsibilities

• Coordinate and support oncology clinical research studies in pediatric hematology/oncology.
• Ensure protocol compliance and assist with regulatory reporting and quality assurance.
• Collect and document accurate clinical data and specimens as required by protocols.
• Serve as liaison among patients, providers, sponsors, and research teams.
• Assist with study life cycle from start-up to closeout.
• Perform informed consent and communicate study updates to the care team.

Skills

Clinical research coordination

GCP compliance

IRB compliance

Data collection

Education

Bachelor's degree in a related field

Job description

The University of Alabama at Birmingham (UAB), Department of Ped - Hematology/Oncology, is seeking a Clinical Research Nurse Coordinator I. The Clinical Research Nurse in Pediatric Hematology/Oncology coordinates and supports oncology clinical research studies involving pediatric patients. This position is responsible for ensuring protocol compliance, coordinating patient care activities related to research participation, collecting and maintaining accurate clinical data and specimens, and serving as a liaison between patients, providers, sponsors, and research teams. The role also supports regulatory compliance, quality assurance, and adherence to Good Clinical Practice (GCP), IRB, and sponsor requirements to ensure the successful conduct of oncology clinical trials.

General Responsibilities

• To 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.
• To support protocol screening and study participant eligibility determination, working with more senior study team members to ensure compliance.
• To 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.
• To coordinate and organize 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 among the clinical and research staff, departments, ancillary services and the study sponsor to ensure protocol compliance throughout the study.

Key Duties & Responsibilities

• Coordinates and manages clinical care activities for pediatric hematology/oncology patients enrolled in oncology research protocols, ensuring compliance with study requirements and institutional guidelines.
• Collects, documents, and maintains accurate clinical research data, specimens, and source documentation required for oncology research studies and regulatory reporting.
• Monitors patient progress throughout research participation, including scheduling study-related appointments.
• Monitors patient progress throughout research participation, including scheduling study-related procedures, assessing protocol adherence, and communicating with physicians, sponsors, and interdisciplinary teams regarding patient care and study updates.
• Ensures compliance with federal regulations, IRB requirements, sponsor guidelines, and Good Clinical Practice (GCP) standards while supporting quality assurance and audit readiness for oncology clinical trials
• Performs other duties as assigned.

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

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.

UAB is an Equal Employment/Equal Educational Opportunity Institution dedicated to providing equal opportunities and equal access to all individuals regardless of race, color, religion, ethnic or national origin, sex (including pregnancy), genetic information, age, disability, and veteran's status. As required by Title IX, UAB prohibits sex discrimination in any education program or activity that it operates. Individuals may report concerns or questions to UAB's Assistant Vice President and Senior Title IX Coordinator. The Title IX notice of nondiscrimination is located at uab.edu/titleix.

Organization

311652600 Ped - Hematology/Oncology

Employee Status

Regular

Shift

Day/1st Shift

Work Arrangement (final schedule to be determined by the department/hiring manager)

Onsite