Clinical Research Coordinator Team Lead - Spartanburg, SC

Requirements

• Coordinate with PI, department, and administration to ensure compliance with federal regulations and sponsor policies.
• Assist PI with study feasibility assessments and protocol review.
• Prepare and maintain study materials, regulatory binders, and source documentation.
• Train and supervise CRCs and research assistants; maintain training logs.
• Develop and implement recruitment strategies in line with IRB requirements.
• Conduct informed consent processes and maintain accurate documentation.
• Manage investigational drug/device accountability and study supply inventory.
• Track enrollment, maintain timelines, and communicate effectively with sponsors and participants.
• Review and approve budget negotiations; attend weekly leadership meetings.
• Act as liaison between site coordinators and research leadership team.

Benefits

• Med/Dent/Vision plus ancillary benefits
• Vacation/PTO
• 401k