Clinical Trials Program Coordinator

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

Job summary

The Medical University of South Carolina is seeking a Program Coordinator I to support clinical research trials under supervision, coordinating daily activities and ensuring compliance and data integrity. You will assist investigators, manage study visits, regulatory submissions, data capture, and communications among sponsors, PI, vendors and hospital services.

Minimum qualifications include a bachelor's degree and 2 years in a related role; strong organizational and communication skills are

Qualifications

• Minimum requirements include a bachelor's degree and two years of relevant program experience.
• Experience coordinating clinical trials and regulatory submissions is preferred.
• Familiarity with Good Clinical Practice guidelines is advantageous.

Responsibilities

• Develops recruitment strategies and engages community physicians to support trial enrollment.
• Screens participants and trains staff on study procedures and documentation.
• Maintains study documentation and ensures compliance with IRB and regulations.
• Uses EDC systems to enter data and supports data quality control processes.
• Coordinates study visits, adverse events, and safety reporting under supervision.

Skills

SPARQ

eIRB

Excel

Communication

Problem-solving

Organizational skills

Clinical trial coordination

Education

Bachelor's degree

Job description

The Medical University of South Carolina is seeking a Program Coordinator I to support clinical research trials under supervision, coordinating daily activities and ensuring compliance and data integrity. You will assist investigators, manage study visits, regulatory submissions, data capture, and communications among sponsors, PI, vendors and hospital services.

Minimum qualifications include a bachelor's degree and 2 years in a related role; strong organizational and communication skills are