Job Title: CRC

Work Location: Chatham County, Georgia

Summary:

This position is responsible for coordinating all aspects of clinical trials, ensuring strict adherence to ICH, GCP, protocol, and regulatory guidelines. The role involves patient coordination, data management, safety assessments, and supporting protocol development activities.

Responsibilities:

• Coordinate patient involvement and study activities for multiple or complex clinical trials from initiation to completion under supervision.
• Organize and manage research information and documentation related to clinical trials.
• Observe study subjects, assist with data analysis, and contribute to reporting processes.
• Schedule and oversee the collection of study data, ensuring accuracy and timeliness.
• Review and report adverse events, protocol deviations, and unanticipated problems as required.
• Monitor research data to maintain quality and compliance with regulatory standards.
• Perform administrative and regulatory duties, including maintaining study records and supporting protocol development.
• Educate participants and caregivers on protocol details, and perform safety and efficacy assessments as assigned.

Qualifications:

• Demonstrated mastery of Clinical Research Coordinator I responsibilities.
• High school diploma or equivalent required; Bachelor’s degree preferred.
• CCRC certification preferred.
• 2-3 years of experience in the medical field preferred.
• Knowledge of federal regulations related to human subjects and clinical trial conduct.
• Strong leadership, mentorship, and crisis management skills.
• Ability to develop and maintain effective working relationships at all organizational levels, including sponsors and vendors.
• Excellent verbal and written communication skills; ability to work independently and as part of a team.

Published Category: Clinical Operations & Development