Oncology Trials Coordinator - Community Sites

Medical University of South Carolina; Charleston (SC); On-site; USD 30,000 - 51,000; Full time

Job summary

Medical University of South Carolina (MUSC) seeks a Clinical Trials Coordinator to support oncology trials across MUSC Florence and community sites. You will coordinate complex protocols, enroll patients, and ensure data quality in CTMS/EPIC systems, while promoting the program within community sites.

You will collaborate with physicians, nurses, and staff to manage eligibility, treatment plans,follow-up, and adverse event reporting in line with NCI and sponsor requirements.

Qualifications

• A bachelor's degree and two years of relevant program experience.

Responsibilities

• Coordinates patient research related activities to meet protocol requirements.
• Assists investigators to identify, consent, screen, and enroll eligible patients.
• Collects and submits data to established research bases including sponsors.
• Maintains up-to-date protocol information and supports study startup and amendments.
• Submits adverse events and other reports to sponsors and IRB per guidelines.

Skills

Clinical research coordination

Regulatory compliance

Data collection

Education

Bachelor's degree

Tools

EPIC

CTMS

Sharepoint

CDC

Job description

Medical University of South Carolina (MUSC) seeks a Clinical Trials Coordinator to support oncology trials across MUSC Florence and community sites. You will coordinate complex protocols, enroll patients, and ensure data quality in CTMS/EPIC systems, while promoting the program within community sites.

You will collaborate with physicians, nurses, and staff to manage eligibility, treatment plans,follow-up, and adverse event reporting in line with NCI and sponsor requirements.