Clinical Research Coordinator I: Study Ops & Data

Medical University of South Carolina; Charleston, Northern (SC, KY); Hybrid; USD 45,000 - 77,000; Full time

Job summary

Medical University of South Carolina in Charleston seeks a Research Coordinator to provide technical and professional services within the SCTR Research Nexus, assisting PIs with coordination of human subject activities and regulatory oversight.

You will lead recruitment, schedule visits, collect data, manage regulatory files, ensure IRB compliance, and collaborate with sponsors, vendors, and hospital services to support multi-site clinical trials.

Qualifications

• Bachelor's degree and at least two years of relevant research experience.
• Knowledge of Good Clinical Practice and human subjects protections.
• Experience with regulatory submissions and IRB processes.
• Proficiency with data collection and EDC systems.

Responsibilities

• Develops recruitment strategies and tools to enroll participants.
• Screens participants and maintains study documentation.
• Oversees regulatory submissions and reporting across sites.
• Manages data collection and entry in EDC systems.
• Supports study visits scheduling and participant safety.
• Ensures compliance with IRB and Good Clinical Practice.
• Collaborates with PI, vendors, and research teams.

Skills

Recruitment planning

Data collection

Regulatory compliance

IRB coordination

Education

Bachelor's degree

Two years of related experience

Tools

EDC platforms

Regulatory submission portals

Job description

Medical University of South Carolina in Charleston seeks a Research Coordinator to provide technical and professional services within the SCTR Research Nexus, assisting PIs with coordination of human subject activities and regulatory oversight.

You will lead recruitment, schedule visits, collect data, manage regulatory files, ensure IRB compliance, and collaborate with sponsors, vendors, and hospital services to support multi-site clinical trials.