Job Title: CRC

Work Location: DeKalb County, Georgia

Summary:

Coordinate all aspects of clinical trials, ensuring strict adherence to ICH, GCP, protocol, and regulatory guidelines. Manage high-volume clinical trial activities, support patient involvement, and maintain compliance throughout the study lifecycle.

Responsibilities:

• Coordinate patient involvement and study activities for multiple or complex clinical trials from initiation to completion.
• Organize and manage research information and documentation related to clinical trials.
• Assist with data collection, analysis, and reporting, including observation of study subjects.
• Monitor, review, and report adverse events, protocol deviations, and unanticipated problems to ensure compliance.
• Perform administrative and regulatory duties, including scheduling and maintaining study records.
• Support protocol development activities and ensure accurate communication of study information and supplies.
• Educate participants and caregivers on protocol details and perform safety and efficacy assessments as required.
• Assist with oversight of vendors, regulatory processes, recruitment, and quality assurance, and contribute to staff training and development.

Qualifications:

• Experience as a Clinical Research Coordinator I or equivalent, with demonstrated mastery of 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 and with external partners.
• Excellent verbal and written communication skills; ability to work independently and as part of a team.
• Ability to manage emergent situations calmly and effectively.
• Willingness to work flexible hours, including up to 50 hours per week as needed, and travel overnight for training or meetings.
• Physical ability to sit, type, stand, walk, and occasionally lift up to 20 pounds.

Published Category: Clinical Operations & Development