Clinical Research Coordinator I

C001 Medical University of South Carolina (MUSC - Univ); Town of Charleston (NY); Sur place; USD 46 000 - 79 000; Plein temps

Résumé du poste

Medical University of South Carolina (MUSC - Univ) seeks a dedicated research coordinator to ensure adherence to study guidelines, coordinate visits, and manage regulatory aspects across multiple studies. You will recruit participants, communicate with Principal Investigators, and prepare audit documents.

The role requires strong computer skills (EPIC, Word, Excel), knowledge of IRB policies, and certifications in biomedical research and Good Clinical Practice.

Qualifications

• Bachelor's degree and two years of relevant program experience.
• CITI certifications in Biomedical Research and Good Clinical Practice; CCRT certification.
• Experience coordinating clinical trials involving drugs, devices, procedures.

Responsabilités

• Maintain up-to-date knowledge of all assigned research projects and report to PI monthly.
• Schedule complex, multi-step study procedures across departments and with sponsors.
• Manage study-specific data and identify data discrepancies.
• Coordinate IRB communications and assist with submissions and amendments.

Connaissances

Communication

Research skills

Time management

Independence

Flexibility

Formation

Bachelor's degree

Outils

EPIC

Word

Excel

Database software

Description du poste

Medical University of South Carolina (MUSC - Univ) seeks a dedicated research coordinator to ensure adherence to study guidelines, coordinate visits, and manage regulatory aspects across multiple studies. You will recruit participants, communicate with Principal Investigators, and prepare audit documents.

The role requires strong computer skills (EPIC, Word, Excel), knowledge of IRB policies, and certifications in biomedical research and Good Clinical Practice.