Pediatric Precision Medicine Trials Coordinator

Medical University of South Carolina; United States; On-site; USD 53,000 - 90,000; Full time

Job summary

The Clinical Trials Office at MUSC in Charleston is seeking a Pediatric Precision Medicine Coordinator to support oncology trials across Hollings Cancer Center and Shawn Jenkins Children’s Hospital. You will coordinate protocol and data management, participant enrollment, and biospecimen operations under supervision.

You will collaborate with clinical operations, data core, lab, IT, pathology, and investigators to ensure timely data submission, quality oversight, and trial continuity.

Qualifications

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

Responsibilities

• Submit complete, accurate data to the Children’s Oncology Group and sponsors.
• Maintain research records, source documents, CRFs, logs, and adverse events.
• Perform chart abstraction and resolve queries within protocol timelines.
• Support data quality reviews and monitoring activities.
• Coordinate consent, enrollment, follow-up, and off-study requirements.
• Maintain participant status in CTMS and EMR with timely updates.
• Participate in CRG clinics and tumor boards to identify participants.
• Coordinate biospecimen collection, processing, and submission per protocol.
• Support program development and cross-functional projects.
• Promote teamwork and ensure training and credential upkeep.

Skills

Clinical data management

Clinical research coordination

Biospecimen handling

EMR/CTMS proficiency

Education

Bachelor's degree

Tools

CTMS

EMR

Job description

The Clinical Trials Office at MUSC in Charleston is seeking a Pediatric Precision Medicine Coordinator to support oncology trials across Hollings Cancer Center and Shawn Jenkins Children’s Hospital. You will coordinate protocol and data management, participant enrollment, and biospecimen operations under supervision.

You will collaborate with clinical operations, data core, lab, IT, pathology, and investigators to ensure timely data submission, quality oversight, and trial continuity.