Clinical Research Coordinator I - Cardiology Trials

Medical University of South Carolina; Charleston (SC); On-site; USD 46,000 - 79,000; Full time

Job summary

Medical University of South Carolina in Charleston is seeking a research coordinator to ensure adherence to study guidelines, coordinate visits, recruit and educate participants, and manage regulatory aspects across multiple studies. You will maintain databases, prepare documents, and liaise with PIs and sponsors for audits.

The role requires strong communication, data management, and IRB process knowledge, with some weekend/evening hours potentially required. Equal opportunity employer.

Qualifications

• Bachelor’s degree and two years of relevant program experience.
• Excellent communication and research skills.
• Strong computer skills: EPIC, Word, Excel, and database software.
• Knowledge of MUSC IRB policies and procedures.
• Required certifications: CITI Biomedical Research and Good Clinical Practice, CCRT, and shipping hazardous materials.
• Experience coordinating clinical trials involving drugs, devices, and procedures.
• Able to work flexible hours; some weekends/evenings may be required.

Responsibilities

• Maintain up-to-date knowledge of all assigned research projects; report monthly to PI and Research Manager; recruit subjects and conduct visits per protocol.
• Schedule complex, multi-step study procedures; coordinate with departments, physicians, and sponsor.
• Manage study‑specific data and identify data discrepancies.
• Coordinate reporting with IRB and sponsor; assist with initial IRB submissions and amendments.

Skills

Communication

Time management

Independent work

Research skills

Attention to detail

Team collaboration

Education

Bachelor’s degree + 2 years experience

Tools

EPIC

Word

Excel

Database software

Email

Job description

Medical University of South Carolina in Charleston is seeking a research coordinator to ensure adherence to study guidelines, coordinate visits, recruit and educate participants, and manage regulatory aspects across multiple studies. You will maintain databases, prepare documents, and liaise with PIs and sponsors for audits.

The role requires strong communication, data management, and IRB process knowledge, with some weekend/evening hours potentially required. Equal opportunity employer.