Clinical Research Coordinator

Clinical Research Coordinator role at ICON in McComb, Mississippi, involving coordination and execution of clinical trials, regulatory compliance, and participant management. The position requires a bachelor's degree in a scientific or healthcare field and prior clinical research experience.

Responsibilities Facilitate coordination and execution of clinical research studies including participant recruitment and enrollment Collaborate with principal investigators, study sponsors, and regulatory authorities on protocol and compliance matters Collect, maintain, and document clinical trial data including adverse events and protocol deviations Manage study documentation such as informed consent forms, case report forms, and regulatory submissions Provide support and education to study participants throughout the research process Requirements Bachelor's degree in relevant scientific or healthcare-related field Previous experience in clinical research or healthcare settings Knowledge of FDA/EMA regulations, ICH-GCP guidelines, and HIPAA Strong organizational, communication, and interpersonal skills Detail-oriented with ability to manage multiple priorities simultaneously Legal right to work in the United States