Regulatory Clinical Research Assistant

MUSC Health; Charleston (SC); On-site; USD 38,000 - 61,000; Full time

Job summary

The Medical University of South Carolina (MUSC) is seeking a Clinical Research Assistant to support the regulatory team, maintaining study documentation and ensuring compliance across regulatory processes. You will coordinate with investigators, IRB, and sponsors to keep studies in good standing.

Responsibilities include building electronic regulatory binders, tracking signatures, preparing materials for audits, and assisting with REDCap data tasks. 40 hours/week, hourly compensation.

Qualifications

• High school diploma plus at least 3 years of relevant program experience.
• Bachelor's degree may substitute for required experience.
• Experience with regulatory documentation is preferred.

Responsibilities

• Manage regulatory documentation files and keep CVs, licensure, training, and certifications up to date.
• Build electronic regulatory binders, route documents for signature, and prepare for audits.
• Schedule and set up monitoring visits; assist with annual continuing reviews.
• Assist with Source Database building in REDCap.
• Provide general office support as needed.

Skills

Regulatory documentation

Attention to detail

Communication

Education

High school diploma

Bachelor's degree acceptable

Tools

REDCap

Job description

The Medical University of South Carolina (MUSC) is seeking a Clinical Research Assistant to support the regulatory team, maintaining study documentation and ensuring compliance across regulatory processes. You will coordinate with investigators, IRB, and sponsors to keep studies in good standing.

Responsibilities include building electronic regulatory binders, tracking signatures, preparing materials for audits, and assisting with REDCap data tasks. 40 hours/week, hourly compensation.