Senior Clinical Trials Coordinator

Medical University of South Carolina; 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 and coordinate phase I-IV clinical trials, ensuring adherence to study protocols and GCP guidelines.

You will collaborate with the program manager and cross-functional teams to handle IRB/IBC submissions, study budgets, contracts, and data management, while mentoring junior staff and maintaining essential documentation in CTMS/EPIC.

Qualifications

• A bachelor’s degree and four years of relevant program experience.
• Experience coordinating clinical trials and regulatory submissions.
• Knowledge of GCP guidelines and regulatory requirements.

Responsibilities

• Coordinate IRB/IBC submissions and regulatory documents.
• Review budgets and contracts with internal departments.
• Schedule visits and assessments per protocol and ensure data integrity.
• Maintain study logs and essential documentation in CTMS/EPIC.
• Mentor junior staff and provide training as needed.
• Support site staff with study procedures and regulatory compliance.

Skills

Regulatory coordination

IRB submissions

Budget review

Data management

GCP compliance

Mentorship

Study documentation

Education

Bachelor’s degree

Tools

EPIC

CTMS

Job description

Medical University of South Carolina seeks a Program Coordinator II to manage and coordinate phase I-IV clinical trials, ensuring adherence to study protocols and GCP guidelines.

You will collaborate with the program manager and cross-functional teams to handle IRB/IBC submissions, study budgets, contracts, and data management, while mentoring junior staff and maintaining essential documentation in CTMS/EPIC.