Oncology Clinical Trials Coordinator

UCLA Health and David Geffen School of Medicine; Orangeburg (SC); On-site; USD 45,000 - 77,000; Full time

Job summary

Medical University of South Carolina (MUSC) seeks a Research Study Coordinator to support oncology trials at Orangeburg and Charleston. The role coordinates, establishes, and supervises complex research protocols and actively promotes the clinical trial program across community sites.

Responsibilities include patient enrollment, eligibility assessment, and timely data entry into CTMS and EPIC, with strict adherence to regulatory reporting and protocol requirements.

Qualifications

• Bachelor's degree required.
• Two years of relevant program experience.
• Experience coordinating complex research protocols preferred.

Responsibilities

• Coordinate and supervise complex oncology trials at MUSC Orangeburg and Charleston.
• Screen, enroll, and manage study participants per protocol.
• Enter/update participant data into CTMS and EPIC within 24 hours.
• Assist with regulatory reporting including adverse events per guidelines.
• Collaborate with physicians, nurses, and study staff to ensure protocol adherence.

Skills

Coordination

Data entry

Communication

Clinical trials

Education

Bachelor's degree

2 years research experience

Tools

EPIC

CTMS

Sharepoint

Clinical Data Center

Job description

Medical University of South Carolina (MUSC) seeks a Research Study Coordinator to support oncology trials at Orangeburg and Charleston. The role coordinates, establishes, and supervises complex research protocols and actively promotes the clinical trial program across community sites.

Responsibilities include patient enrollment, eligibility assessment, and timely data entry into CTMS and EPIC, with strict adherence to regulatory reporting and protocol requirements.