CLINICAL RESEARCH NURSE COORDINATOR I

UAB Medicine; University (FL); On-site; USD 52,555 - 85,400; Full time

Job summary

UAB Medicine in Florida is seeking a Clinical Research Nurse Coordinator I to oversee oncology clinical research studies in pediatric patients. This role is essential in ensuring protocol compliance, coordinating patient care, and managing clinical research data. Candidates must have a Bachelor's degree and be licensed as a Registered Nurse in Alabama.

The position offers a salary range of $52,555 - $85,400 and requires a commitment to quality assurance in clinical trials.

Qualifications

• Bachelor's degree in a relevant 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.

Responsibilities

• Serve as coordinator for clinical research studies and provide support to other study team members.
• Conduct all study activities in accordance with regulatory requirements and GCP.
• Monitor patient progress throughout research participation.

Skills

Clinical research coordination

Patient care management

Good Clinical Practice (GCP)

Regulatory compliance

Education

Bachelor's degree in a related field

Currently licensed or eligible for RN licensure in Alabama

Job description

CLINICAL RESEARCH NURSE COORDINATOR I (T236456)

The University of Alabama at Birmingham (UAB), Department of Pediatric 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

• Serve as coordinator for clinical research studies and provide 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.
• Assist with the life cycle of the study from start-up through maintenance to closure.
• Coordinate and organize participant care 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.

Key Duties & Responsibilities

1. Coordinate and manage clinical care activities for pediatric hematology/oncology patients enrolled in oncology research protocols, ensuring compliance with study requirements and institutional guidelines.
2. Collect, document, and maintain accurate clinical research data, specimens, and source documentation required for oncology research studies and regulatory reporting.
3. Monitor patient progress throughout research participation, including scheduling study-related appointments.
4. Monitor 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.
5. Ensure 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.
6. Perform other duties as assigned.

Annual Salary Range

$52,555 - $85,400

Qualifications

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.

Primary Location

University

Job Category

Clinical Research

Organization

311652600 Ped - Hematology/Oncology

Employee Status

Regular

Shift

Day/1st Shift

Work Arrangement

Onsite