Position Overview:
The Clinical Research Coordinator (CRC) role requires close collaboration with the principal investigator (PI), study sponsor, and clinical staff to ensure smooth operation of the trial in compliance with regulatory standards.
Key Responsibilities:
- Coordinate and manage the daily operations of the clinical trial, ensuring adherence to the study protocol, good clinical practice (GCP), and regulatory requirements.
- Perform assessments and procedures to support trial data collection.
- Schedule and conduct study visits, including screening, enrollment, and follow-up of participants.
- Collect, process, and manage study data, maintaining accurate and detailed records in the electronic data capture (EDC) system.
- Prepare study materials, including informed consent forms, patient binders, and regulatory documents.
- Communicate with the PI and sponsor regarding trial progress, patient enrollment, and data collection.
- Ensure patient safety and compliance with trial protocols, assisting with adverse event reporting when necessary.
- Manage trial supplies, including ophthalmic instruments and study-related materials.
Qualifications:
- Ophthalmology Technician certification or equivalent experience.
- Proficiency in retina imaging (e.g., OCT, fundus photography).
- Experience as a Clinical Research Coordinator or involvement in clinical trials is highly desirable.
- Excellent organizational skills with the ability to manage multiple tasks and priorities.
Details:
Location: Greater Atlanta, GA
Hours: Full-time, M-F 8 AM - 5 PM, On-Site
Duration: 1040 hours Contracted Period