Clinical Research Coordinator
ICON · MS
Clinical OperationsPart-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
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.
What they're looking for
- 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
What you'll be doing
- 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
Privacy & handoff
This role links to ICON's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.