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MUSC Health·Charleston, SC

UNIV - Program Coordinator I - Department of Medicine: Division of Cardiology

Healthcare AdministrationFull time40 hrs/wk
iPosting details
Schedule40 h/wk · Full time
EducationBachelor's degree
Experience2+ years
SourceMUSC Health · posted Oct 2, 2026
✓Requirements
Certifications
✓Required certifications include CITI certifications in Biomedical Research and Good Clinical Practice , CCRT certification, and shipping hazardous materials.
Education
✓A bachelor's degree and two years of relevant program experience.
Qualifications
✓The position requires excellent communication and research skills. Must have strong computer skills (EPIC, Word, Excel, database software, web based activities, email).
✓This position requires excellent time management, and the ability to work independently. A willingness to work flexible hours is necessary; some weekend and evening work may be required.
Knowledge of MUSC IRB policies and procedures is necessary. preferred
Experience coordinating clinical trials that involve drugs, devices, and procedures is necessary. preferred
+Benefits
✓Flexible scheduling
+MUSC Health
148administration roles open
CharlestonSC · 172 mi to Charlotte
✓You’ll need
Certifications
✓Required certifications include CITI certifications in Biomedical Research and Good Clinical Practice , CCRT certification, and shipping hazardous materials.
Education
✓A bachelor's degree and two years of relevant program experience.
Qualifications
✓The position requires excellent communication and research skills. Must have strong computer skills (EPIC, Word, Excel, database software, web based activities, email).
✓This position requires excellent time management, and the ability to work independently. A willingness to work flexible hours is necessary; some weekend and evening work may be required.
Knowledge of MUSC IRB policies and procedures is necessary. preferred
Experience coordinating clinical trials that involve drugs, devices, and procedures is necessary. preferred
+Benefits
Flexible scheduling

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About the role

This individual will be responsible for ensuring adherence to study guidelines, coordinating study visits, ensuring participants meet stringent clinical inclusion guidelines, and providing education to patients and their families The candidate will be responsible for all regulatory aspects of multiple studies, maintaining study databases, completing study documents, recruiting study patients, communicating with Principal Investigators and sponsors as well as preparing and conducting audits.