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CLINICAL RESEARCH QUALITY COORDINATOR

University of Alabama at Birmingham

University of Alabama at Birmingham

Quality Assurance
university, fl, usa
USD 50,050-81,330 / year
Posted on Nov 18, 2025
CLINICAL RESEARCH QUALITY COORDINATOR - (T231396)

Description

The University of Alabama at Birmingham (UAB), Ped - Hematology/Oncology is seeking a Clinical Research Quality Coordinator. This role ensures the quality and regulatory compliance of clinical research activities within assigned studies and programs. The incumbent will support monitoring and auditing of quality assurance processes and provide guidance to research teams to ensure adherence to institutional, sponsor, and federal requirements. Establishing this position is essential to maintaining consistent compliance standards across multiple trials, minimizing regulatory risk, and supporting the division's expanding research portfolio.

General Responsibilities

  • To ensure the quality and regulatory compliance of clinical research activities assigned to studies or programs.

  • To support the monitoring and auditing of quality assurance processes and provide guidance to research teams to ensure adherence to institutional and federal requirements.

Key Duties & Responsibilities

  1. Provides ongoing remote clinical monitoring assistance to study sites.

  2. Provides ongoing monitoring and review of safety reporting as follows, but not limited to: review of all adverse events documented by site CRAs into the study database/eDES. Review of all reporting of SAE via eDES, Medwatch Report Forum, and Pharmaceutical documents, and provide assistance as needed.

  3. Safety reporting to Sponsor, Protocol Chair, Protocol Team, Operations Center PI, Medical Monitor, DSMB, Study sites, and other protocol-designated agencies into eDES, along with email prompts for delinquent data entries.

  4. Provides monitoring review of all newly screened and potential study participants.

  5. Provides ongoing protocol training/support to clinical sites.

  6. Monitors and reviews all central evaluations and sends evaluations to study sites and summarizes protocol requirements as needed.

  7. Collects all external IND safety reports.

  8. Obtains Operations Center Pl's written acknowledgement.

  9. Obtains Protocol Chair's written acknowledgement.

  10. Maintains a safety log of all received safety reports and specifies when protocol and/or consent document changes are required.

  11. Shares all external IND safety reports with clinic study sites after obtaining the Protocol Chair's written acknowledgement.

  12. Places all external IND safety report email communication to clinical sites into eDES study-specific docs section folder.

  13. Works with the regulatory specialist whenever changes to the informed consent document are required. Plexiform QOL review and site queries.

  14. Reviews of diary drug compliance documents generate queries when necessary. NF Consortium email requests for assistance (potential subjects). Protocol Reviews participate in all protocol reviews and editing if needed. Travel to sites/travel expected 1 to 2 times per month for an average of 1-2 days per monitoring visit or 1 week per month.

  15. Follows the QAC Guidelines for site monitoring. Remote Monitoring - since COVID, remote monitoring.

  16. Provides recommendations of notes to files, provides documentation, and is available for internal audits.

  17. Handles protocol clinical queries by sites and delinquent queries to the site for missing data.

  18. Reports to the QAC Chair as appropriate.

  19. Drug accountability, maintenance, and compliance overall study and final study reports.

  20. Coordinates with Pharmacy for drug compliance. Keep up-to-date database clinical records

  21. Performs other duties as assigned.

Annual Salary Range: $50,050 - $81,330

Qualifications

Bachelor's degree in a related field and three (3) years of related experience required. Work experience may substitute for education requirement.

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 (final schedule to be determined by the department/hiring manager): Remote/Hybrid Eligible