Clinical Research Program Coordinator I

Medical University of South Carolina; Orleans Estates (SC); On-site; USD 45,300 - 77,000; Full time

Job summary

Medical University of South Carolina in the United States seeks a Program Coordinator I to assist investigators in initiating, coordinating, and managing clinical trials. You will support daily trial activities, ensure compliance, and provide guidance to investigators, faculty and staff.

Under supervision, you will develop recruitment, screen participants, manage data, and help prepare regulatory submissions. This role offers 40 hours weekly in a research grant environment.

Qualifications

• Bachelor's degree required with at least two years of relevant program experience.
• Experience coordinating clinical research studies and knowledge of regulations is preferred.
• Ability to prepare regulatory submissions and maintain study registrations.

Responsibilities

• Assist with initiation, coordination and management of clinical trials.
• Develop recruitment strategies and engage physicians and community partners.
• Screen participants and oversee study team training on study procedures.
• Document subject data and ensure compliance with GCP and regulatory requirements.
• Prepare safety reports and assist with IRB submissions and study monitoring.

Skills

Research coordination

Regulatory submissions

Data management

Communication

IRB knowledge

Education

Bachelor's degree

Tools

ClinicalTrials.gov

Job description

Medical University of South Carolina in the United States seeks a Program Coordinator I to assist investigators in initiating, coordinating, and managing clinical trials. You will support daily trial activities, ensure compliance, and provide guidance to investigators, faculty and staff.

Under supervision, you will develop recruitment, screen participants, manage data, and help prepare regulatory submissions. This role offers 40 hours weekly in a research grant environment.