Clinical Trials Program Coordinator II

UCLA Health and David Geffen School of Medicine; Charleston (SC); On-site; USD 53,000 - 90,000; Full time

Job summary

Medical University of South Carolina seeks a Program Coordinator II to manage study-related procedures for patients in phase I–IV clinical trials. Under the supervision of the Program Manager, you will ensure compliance with protocols, regulatory requirements, and GCP guidelines, while coordinating IRB submissions and site communications.

The role requires a bachelor’s degree and four years of related program experience, with responsibilities spanning data handling, budgeting, and staff

Qualifications

• Bachelor's degree required with four years of relevant program experience.

Responsibilities

• Coordinate and manage clinical trials ensuring protocol compliance and GCP guidelines.
• Submit IRB and IBC documents as required.
• Review budgets and contracts with program manager and internal departments.
• Schedule and conduct study visits and assessments per protocol.
• Maintain CTMS systems and ensure accurate EPIC billing charges.
• Mentor junior staff and serve as a resource for study procedures.

Skills

Clinical trial coordination

GCP compliance

IRB submissions

Budget & contracts review

Education

Bachelor's degree

Tools

EPIC

CTMS

Job description

Medical University of South Carolina seeks a Program Coordinator II to manage study-related procedures for patients in phase I–IV clinical trials. Under the supervision of the Program Manager, you will ensure compliance with protocols, regulatory requirements, and GCP guidelines, while coordinating IRB submissions and site communications.

The role requires a bachelor’s degree and four years of related program experience, with responsibilities spanning data handling, budgeting, and staff