Remote: Entry-Level Clinical Research Regulatory Coordinator

University of Alabama at Birmingham; University (FL); Hybrid; USD 26,000 - 42,000; Full time

Job summary

The University of Alabama at Birmingham invites applications for the Clinical Research Regulatory Coordinator I. This role supports regulatory activities for clinical studies, including industry-sponsored, federally funded, and investigator-initiated projects.

Responsibilities include preparing IRB submissions, maintaining regulatory documents, managing consent forms and delegation logs, and ensuring compliance with GCP and institutional policies.

Qualifications

• High School diploma or GED is required.
• Familiarity with IRB processes or regulatory documentation is a plus.
• Strong computer skills, including Microsoft Office.

Responsibilities

• Maintain regulatory documentation (consent forms, protocols, 1572s, CVs, licenses, brochures, recruitment materials, safety reports, submission forms).
• Prepare IRB submissions with relevant documents and signatures to meet study timelines.
• Draft initial informed consent documents as needed.
• Prepare regulatory binders and related documentation.

Skills

Clinical research

Regulatory experience

IRB processes

Microsoft Office

Education

High School diploma or GED

Tools

Microsoft Office

Job description

The University of Alabama at Birmingham invites applications for the Clinical Research Regulatory Coordinator I. This role supports regulatory activities for clinical studies, including industry-sponsored, federally funded, and investigator-initiated projects.

Responsibilities include preparing IRB submissions, maintaining regulatory documents, managing consent forms and delegation logs, and ensuring compliance with GCP and institutional policies.