Clinical Trials Coordinator II: GCP & IRB Focus

Medical University of South Carolina; Charleston (SC); On-site; USD 53,000 - 90,000; Full time

Job summary

The Medical University of South Carolina is seeking a Program Coordinator II to manage phase I–IV clinical trials under the Program Manager, ensuring protocol compliance and high-quality data collection.

Key duties include IRB/IBC submissions, budgeting reviews with the program team, scheduling visits, and maintaining study documentation. This full-time on-site role requires strong regulatory knowledge and mentorship capabilities in Charleston, SC.

Qualifications

• Bachelor's degree and four years of relevant program experience.
• Experience coordinating clinical trials and regulatory compliance.
• Knowledge of GCP and ALCOA++ data integrity.

Responsibilities

• Coordinate and manage clinical trials per study protocol.
• Submit required IRB/IBC applications and responses.
• Review budgets and contracts with the program manager.
• Schedule and conduct study visits and assessments.
• Maintain and reconcile CTMS/EPIC billing and study charges.
• Mentor junior staff and provide training.
• Serve as a liaison between site staff, sponsors and vendors.

Skills

Clinical trial coordination

Regulatory compliance

GCP ALCOA++ data integrity

Mentorship/training

Education

Bachelor's degree

Tools

EPIC

CTMS

Job description

The Medical University of South Carolina is seeking a Program Coordinator II to manage phase I–IV clinical trials under the Program Manager, ensuring protocol compliance and high-quality data collection.

Key duties include IRB/IBC submissions, budgeting reviews with the program team, scheduling visits, and maintaining study documentation. This full-time on-site role requires strong regulatory knowledge and mentorship capabilities in Charleston, SC.