Senior Clinical Research Coordinator — Complex Trials

MUSC Health; Charleston (SC); On-site; USD 45,300 - 77,000; Full time

Job summary

The Senior Clinical Research Coordinator at the Medical University of South Carolina (MUSC - Univ) coordinates day-to-day conduct of complex clinical studies in adherence with GCP, policies, and regulations. This role supports disease-specific workflows, maintains study data and documentation, and prepares monitoring/audit materials.

The position requires collaboration with investigators, sponsors, and regulatory partners, with potential after-hours visits and some travel for meetings.

Qualifications

• Bachelor's degree and 3 years of relevant program experience.
• Experience coordinating clinical studies per GCP and regulations.

Responsibilities

• Coordinate assigned protocols and study visits per protocol.
• Screen and enroll participants and obtain informed consent.
• Monitor adverse events and report serious events.
• Collect, enter, and manage data in study databases.
• Support sponsor monitors, audits, and regulatory inspections.
• Mentor staff and communicate with investigators and vendors.

Skills

Epic Systems

Study coordination

Education

Bachelor's degree

Tools

EPIC

Job description

The Senior Clinical Research Coordinator at the Medical University of South Carolina (MUSC - Univ) coordinates day-to-day conduct of complex clinical studies in adherence with GCP, policies, and regulations. This role supports disease-specific workflows, maintains study data and documentation, and prepares monitoring/audit materials.

The position requires collaboration with investigators, sponsors, and regulatory partners, with potential after-hours visits and some travel for meetings.