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Medical University of South Carolina

Health sciences university in Charleston, SC

Regulatory Coordinator - Department of Medicine: Division of Pulmonary

Full-TimeUpdated on 10/23/2026
$45.3k - $77k
Junior
Bachelor's
Charleston, SC, USA
In Person
Biology & BiotechClinical Research Operations

About the job

Requirements
  • A bachelor's degree and one year of relevant program experience are required.
  • The role requires the ability to perform the listed physical functions, including frequent sitting, walking/mobile activity, fine motor movements, and lifting, carrying, lowering, or pushing/pulling objects up to 15 pounds on an infrequent basis.
  • The role requires the ability to work indoors continuously and outdoors in all weather and temperature extremes infrequently.
  • The role requires corrected vision of 20/40 in at least one eye, distance and depth perception, peripheral vision, and hearing acuity, with correction.
Responsibilities
  • Coordinate and perform study-specific regulatory processes for the Clinical Trial Research Program, ensuring deadlines are met and regulations and standard operating procedures are followed.
  • Receive sponsor start-up packets and initiate and monitor study start-up activities and required documentation.
  • Submit study amendments and changes to the institutional review board (IRB) upon activation, notify the study team of approvals, and submit continuing reviews.
  • Answer questions and provide documents requested by the investigator, program manager, and study sponsor.
  • Maintain accurate study registrations, including ClinicalTrials.gov, for investigator-initiated projects, and provide guidance on re-consenting subjects and reporting events under IRB policy.
  • Maintain regulatory documentation, including curricula vitae, medical licensure, note-to-files, conflict-of-interest documents, laboratory certifications, and other required records.
  • Build electronic regulatory binders and maintain electronic files.
  • Oversee regulatory documentation for multi-site projects when MUSC is the lead site and create templates for use by those projects.
  • Create and maintain the eSource documentation database for research coordinators for the full study lifecycle, from creation through closure.
  • Code and build source structures, edit fields based on protocol amendments or usage needs, create reports and alerts, and notify the study team of changes.
  • Ensure documents are complete and filed in the regulatory binder, physically or electronically.
  • Work with study monitors to resolve action items promptly and review corrective action plans with the Regulatory Manager to ensure issues are addressed.
  • Maintain familiarity with central institutional review boards (CIRBs), keep current on their processes and application changes, and maintain site-level CIRB policies for reference.
  • Provide administrative support to the Program Manager, Accountant Fiscal Manager, Education & Operations Specialist, Accountant/Fiscal Analyst, and Regulatory Manager, including scheduling meetings, assisting with program events, and conducting site tours.
  • Complete IRB and/or sponsor-reportable events independently and apply protocol and institutional guidelines to distinguish reportable from non-reportable adverse events.
  • Assist with other study tasks or projects as needed.

About the company

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Medical University of South Carolina

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Medical University of South Carolina is a public academic health sciences university in Charleston, South Carolina. It offers bachelor's, master's, doctoral, and professional degrees through six colleges in dental medicine, graduate studies, health professions, medicine, nursing, and pharmacy.

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