Oncology Clinical Trials Coordinator

Medical University of South Carolina; Orleans Estates (SC); On-site; USD 46,000 - 78,000; Full time

Job summary

Medical University of South Carolina (MUSC) seeks a research coordinator to support Hollings Cancer Center oncology trials. You will coordinate complex protocols, manage patient study participation, and promote the trial program within HCC while ensuring protocol adherence and participant safety.

The role involves data entry into CTMS/EPIC, coordination with physicians and nurses, and timely reporting of study activities. A bachelor’s degree and clinical research experience are required.

Qualifications

• Bachelor's degree and two years of relevant program experience.
• Experience with clinical trials data entry and CTMS tools.
• Knowledge of oncology terminology is helpful but not required.

Responsibilities

• Coordinates patient research activities to meet protocol requirements and updates CTMS/EPIC within 24 hours.
• Assists investigators to identify, screen, and enroll eligible patients for trials.
• Collects and submits data to NCI, sponsors, and MUSC with timely accuracy.
• Prepares and submits adverse events and protocol deviations per guidelines.
• Maintains up-to-date protocol information and supports startup and amendments.

Skills

Clinical research coordination

Patient management

Regulatory knowledge

Education

Bachelor's degree

Two years relevant program experience

Tools

EPIC

CTMS

SharePoint

Clinical Data Center

Job description

Medical University of South Carolina (MUSC) seeks a research coordinator to support Hollings Cancer Center oncology trials. You will coordinate complex protocols, manage patient study participation, and promote the trial program within HCC while ensuring protocol adherence and participant safety.

The role involves data entry into CTMS/EPIC, coordination with physicians and nurses, and timely reporting of study activities. A bachelor’s degree and clinical research experience are required.