Clinical Research Coordinator I — Center for Innovation

Brooks Rehabilitation; Jacksonville (FL); On-site; USD 45,000 - 65,000; Full time

Job summary

Brooks Rehabilitation in Jacksonville, FL is seeking a proactive Clinical Research Coordinator I (CRC-I) to support the Brooks Center for Innovation. You will assist in data collection, documentation, and analysis across assigned protocols and help maintain current reporting and tracking information.

Under supervision of Principal Investigators and senior staff, you may coordinate regulatory processes, conduct recruitment, screenings, informed consent, and study procedures while ensuring

Qualifications

• Bachelor’s degree required; 1 year of research experience preferred.
• Strong planning, management, organizational and communication skills.
• Knowledge of state/federal rules governing clinical research preferred.
• CPR certification required.

Responsibilities

• Assist in preparing for study monitoring or auditing visits.
• Assist study personnel in conducting study procedures.
• Conduct informed consent and initial screenings with potential participants.
• Document AE/SAEs and communicate to study personnel.
• Identify situations needing PI involvement.
• Input data and maintain study documentation per procedures.
• Maintain study metrics and training/certifications.
• Plan study sessions and ensure resources are available.
• Prepare documents/equipment/space prior to visits.
• Schedule screening calls/visits and study visits per protocol.
• Serve as primary contact for general study inquiries.
• Assist in developing research contracts and IRB submissions.
• Collaborate with Center for Innovation on literature reviews.

Skills

Planning

Management

Organization

Communication

Collaboration

Analytical

Leadership

Self-motivation

Self-regulation

Verbal/written communication

Education

Bachelor's degree

Tools

Windows

Web-based applications

Job description

Brooks Rehabilitation in Jacksonville, FL is seeking a proactive Clinical Research Coordinator I (CRC-I) to support the Brooks Center for Innovation. You will assist in data collection, documentation, and analysis across assigned protocols and help maintain current reporting and tracking information.

Under supervision of Principal Investigators and senior staff, you may coordinate regulatory processes, conduct recruitment, screenings, informed consent, and study procedures while ensuring