Clinical Research Study Coordinator

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

Job summary

Medical University of South Carolina in Charleston invites applications for a Research Study Coordinator to support pediatric clinical trials. The role involves direct patient contact and coordination with the PI and research team on interventional and observational studies.

You will manage visits, data collection, regulatory filings, and collaboration with vendors, IRB submissions, and trial logistics on-site at MUSC, with a potential remote option after one year.

Qualifications

• Bachelor’s degree and two years relevant program experience.
• Ability to perform in a clinical research setting with regulatory requirements.
• On-site work with potential after-hours and travel.

Responsibilities

• Scheduling and conducting study visits and assessments per protocol.
• Collecting, processing, shipping, and maintaining inventory of research biological specimens.
• Ensuring timely and accurate data collection following GCP and ALCOA++ guidelines.
• Maintaining accurate and up-to-date paper and electronic regulatory files.
• Performing pre-screening activities through screening, medical chart review, and in person discussions with study investigators to aid with recruitment.
• Preparing and creating essential study documents including worksheets, source documents, and study logs.
• Assisting with and completing IRB submissions, including initial submissions, amendments, reportable events, and continuing reviews.
• Serving as the primary liaison between site staff, sponsors, study vendors and other internal departments involved in the conduct of clinical research.

Skills

Clinical research

Data entry

GCP knowledge

IRB submissions

Education

Bachelor’s degree

Tools

EDC systems

Job description

Medical University of South Carolina in Charleston invites applications for a Research Study Coordinator to support pediatric clinical trials. The role involves direct patient contact and coordination with the PI and research team on interventional and observational studies.

You will manage visits, data collection, regulatory filings, and collaboration with vendors, IRB submissions, and trial logistics on-site at MUSC, with a potential remote option after one year.