Clinical Research Coordinator

Key Responsibilities

• Counsels and educates participants about the study.
• Monitors subject safety and reports adverse events.
• Completes source documentation and EDC data entry.
• Solves data queries and ensures data integrity.
• Maintains investigational product accountability and proper storage.
• Prepares for and supports monitoring visits, audits, and inspections.
• Collaborates with site staff and investigators.

Skills/Abilities

• Strong knowledge of medical terminology and clinical procedures.
• Understanding of ICH/GCP and regulatory requirements.
• Excellent organizational skills and attention to detail.
• Strong interpersonal and patient-facing communication skills.
• Ability to multitask and manage competing priorities in a fast-paced environment.
• Proficiency in Microsoft Office, EDC, and CTMS applications.
• Ability to work both independently and collaboratively.
• High level of professionalism and commitment to patient confidentiality.

Education/Experience

• High school diploma required.
• Bachelor’s degree in related field preferred.
• 2+ years of clinical research experience.
• Experience with patient-facing activities (phlebotomy, vital signs, EKGs, etc.) or ophthalmology tasks (OCT imaging, measuring IOP, etc.) strongly preferred.