"CLINICAL RESEARCH DATA COORDINATOR III (PART-TIME)"

CLINICAL RESEARCH DATA COORDINATOR III (PART-TIME)

Posted: 14-Jan-26

Location: Birmingham, Alabama

Type: Regular

Categories: Staff/Administrative

Internal Number: T231879

The University of Alabama at Birmingham (UAB), Ped - Hematology/Oncology, is seeking a Clinical Research Data Coordinator III (Part-Time).

General Responsibilities

• To design, implement, and maintain clinical-based relational database management systems and tools.
• To develop methods for tracking and reporting data and monitors incoming and outgoing data to ensure data integrity and compliance with applicable regulatory agency standards.
• To perform a variety of statistical analyses and summarizes results.
• To manage clinical data warehouse systems and reporting to national data marts to ensure accuracy, security, and compliance.

Key Duties & Responsibilities

1. Verifies compliance with each enrollment and tracks patient compliance throughout the entire duration of the study.
2. Develops methods to track and report data.
3. Conducts quality assurance activities. May compile and analyze data.
4. Develops and implements procedures, maintains records, tracks progress, and conducts quality assurance on data collected.
5. Enters data into REDCap and eDES systems.
6. Completes Case Report Forms (CRF) according to protocol.
7. Documents Adverse Events (AEs) and Serious Adverse Events (SAEs) as required by protocol and regulatory guidance.
8. Collaborates effectively with principal investigators, clinical staff, and research teams to facilitate study operations and protocol adherence.
9. Contributes to team meetings, process improvements, and disseminates research findings through manuscript and presentation support.
10. Attends study, departmental, and institutional trainings and meetings as required.
11. Serves as liaison between UAB staff and other stakeholders.
12. Performs other duties as assigned.

Hourly Range: $26.55 - 43.10

Qualifications

Bachelor's degree in a related field and five (5) years of related experience required. Work experience may NOT substitute for education requirement. Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP) certification preferred.