Senior Clinical Research Coordinator – Study Lead

Medical University of South Carolina; Orleans Estates (SC); On-site; USD 45,000 - 77,000; Full time

Job summary

The Senior Clinical Research Coordinator at the Medical University of South Carolina leads day-to-day coordination of complex clinical studies, ensuring Good Clinical Practice (GCP) compliance and accurate documentation. This role interfaces with investigators, sponsors, participants, families/caregivers, ancillary services, vendors, and regulatory partners to support safe, high-quality study conduct.

You will manage visits, data entry, SAE reporting, and sponsor readiness, with potential

Qualifications

• Bachelor’s degree and three years of relevant program experience.
• Experience coordinating complex clinical research studies.
• Knowledge of GCP, regulatory requirements, and study documentation.

Responsibilities

• Coordinate assigned research protocols and oversee visits per protocol.
• Screen and enroll participants and obtain informed consent.
• Monitor adverse events and prepare SAE reports.
• Collect and manage data, enter CRFs, and maintain compliant study records.
• Prepare for sponsor monitoring visits and audits.
• Mentor junior staff and coordinate with investigators and sponsors.

Skills

Visit coordination

Data management

Regulatory compliance

Study documentation

Education

Bachelor's degree

Tools

Epic

Job description

The Senior Clinical Research Coordinator at the Medical University of South Carolina leads day-to-day coordination of complex clinical studies, ensuring Good Clinical Practice (GCP) compliance and accurate documentation. This role interfaces with investigators, sponsors, participants, families/caregivers, ancillary services, vendors, and regulatory partners to support safe, high-quality study conduct.

You will manage visits, data entry, SAE reporting, and sponsor readiness, with potential