Clinical Research Coordinator

Responsibilities

• Manage the integrity and overall quality of assigned clinical research trials
• Serve as the primary contact for study subjects and sponsors
• Review study protocols and prepare study document binders and source documents
• Perform study procedures including pre-screening, screening, and study visits
• Conduct vital signs, EKG, phlebotomy, and specimen processing
• Document patient progress and complete case report forms
• Coordinate monitor visits and maintain communication with physicians regarding study requirements and adverse events
• Maintain trial regulatory documentation and adhere to ICH/GCP guidelines

Requirements

• Minimum of 2 years of relevant work experience as a Clinical Research Coordinator
• High attention to detail and strong organizational skills
• Excellent verbal and written communication skills
• Proficiency with Electronic Medical Records (EMR)

Preferred Qualifications

• Experience in Neurology
• CCRC certification
• Working knowledge of research methodology, medical terminology, and pharmacology

Benefits

• Competitive Salary
• Generous paid time off
• Medical, Dental, and Vision Insurance