CLINICAL RESEARCH REGULATORY COORDINATOR III

UAB; University (FL); Hybrid; USD 55,000 - 72,000; Full time

Job summary

The University of Alabama at Birmingham (UAB) is seeking a Clinical Research Regulatory Coordinator III to lead complex regulatory activities within the Pulmonary/Allergy/Critical Care division. The role emphasizes reporting metrics, timelines, and coaching junior staff while ensuring adherence to ICH-GCP, FDA, HIPAA, and UAB policies.

Responsibilities include preparing submissions for IRB and FDA filings, overseeing regulatory documentation, and driving quality initiatives across multiple

Qualifications

• Bachelor’s degree plus five years related experience required.
• CCRC or CCRP certification preferred.
• Must understand regulatory requirements for ICH-GCP, FDA, and HIPAA.

Responsibilities

• Prepare and submit IRB applications, amendments, continuing reviews, and reportable events.
• Lead regulatory processes for moderate to complex studies and oversee documentation.
• Coordinate audits, inspections, and corrective action planning.
• Maintain regulatory binders, eISFs, logs and ensure compliance across protocols.

Skills

Project management

Risk assessment

Communication

MS Office

Team collaboration

Education

Bachelor’s degree in a related field

Tools

MURE

IRAP

Florence e-binder

Veeva Vault

Job description

CLINICAL RESEARCH REGULATORY COORDINATOR III – (T237044)

Description

The University of Alabama at Birmingham (UAB), Department of Med – Pulmonary/Allergy/Critical Care, is seeking a Clinical Research Regulatory Coordinator III.

This job position functions as a senior-level regulatory specialist with UAB regulatory expertise. This is considered a lead position, and the candidate must understand he/she is also responsible for reporting metrics (timelines, trends, compliance-related issues), timeliness (meeting deadlines), and providing leadership and/or training to junior staff. Core responsibilities include project oversight, preparation, submission, and tracking of IRB applications (including continuing reviews, amendments, and reportable events). Responsibilities also include documentation oversight (regulatory binders, eISFs, logs, etc.), ensuring all documents meet ICH-GCP, FDA, OHRP, and UAB policies, and compliance monitoring (must be knowledgeable of federal regulations, human subjects protections, HIPAA, and informed consent processes).

++General Responsibilities++

• To prepare and submit multiple levels of research documentation (i.e. IRB submissions, educational materials, reports, grant renewal reports, and study forms).




• To prepares and maintain FDA applications for Investigational New Drugs (INDs) and Investigational Device Exemptions (IDEs).




• To lead the implementation of study specific regulatory processes of a moderate to complex nature.




• To conduct internal quality assurance audits of regulatory files as well as programs, reports, and teams working within clinical trial operations.




• To design and implement quality initiatives ensuring effective and efficient clinical processes.

++Key Duties & Responsibilities++

1. Subject matter expert for complex, high-risk trials and capable of advising investigators and leadership on regulatory processes and risk mitigation.




2. Prepares for and helps lead responses for FDA inspections, audits, quality assurance reviews, and monitoring visits. Identifying compliance gaps and implementing processes for corrective action planning is required.




3. Maintains standardized regulatory practices across multiple studies with multiple PIs is required. Must be competent in using a variety of electronic platforms as well as competent in the knowledge of FDA regulations, HSP, UAB research processes, and IRB submission processes.




4. Performs other duties as assigned.

++Annual Salary Range++

$55,180 – $71,735

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.

++Preferences++

• Have strong project management and risk assessment skills.




• Be able to communicate effectively with staff, investigators, sponsor representatives, legal officers, and other clinical trials administrative staff.




• Possess great computer skills, have experience with Microsoft Office, be able to engage in group meetings and discussions, must be able to actively work closely with others and under the leadership of Investigators and senior research coordinators in a variety of settings, and have a strong work ethic.




• Must also be knowledgeable of UAB systems such as MURE, IRAP, Florence e-binder system, and Veeva Vault.

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

: 311402800 Med – Pulmonary/Allergy/Critical Care

Employee Status

: Regular
Shift: Day/1st Shift
Work Arrangement (final schedule to be determined by the department/hiring manager): Hybrid Eligible