Senior Research Program Coordinator – Clinical Trials

MUSC Health; Charleston (SC); On-site; USD 53,000 - 90,000; Full time

Job summary

Medical University of South Carolina (MUSC - Univ) seeks a Research Program Coordinator II–Journeyman to design and administer complex clinical studies within a university setting. The role requires coordinating protocol processes, liaising with PIs, sponsors and study teams to ensure compliance and data integrity.

The position supports multiple trials, leads day-to-day operations, and ensures IRB and FDA requirements are met.

Qualifications

• Bachelor's degree and three years of relevant program experience.
• Experience coordinating multiple complex research studies.
• Familiarity with IRB, FDA and regulatory documentation.

Responsibilities

• Review and manage research protocols, submissions and IRB approvals.
• Coordinate communication with PI, study staff, sponsors and sub-sites.
• Oversee data collection, adverse event reporting and protocol deviations.
• Maintain regulatory documents, logs and study records across trials.
• Train staff and serve as a subject matter expert on research regulations.

Skills

Program coordination

IRB compliance

Regulatory knowledge

Education

Bachelor's degree

Job description

Medical University of South Carolina (MUSC - Univ) seeks a Research Program Coordinator II–Journeyman to design and administer complex clinical studies within a university setting. The role requires coordinating protocol processes, liaising with PIs, sponsors and study teams to ensure compliance and data integrity.

The position supports multiple trials, leads day-to-day operations, and ensures IRB and FDA requirements are met.