Primary Health Clinical Research Coordinator (Non-Lab)

• Coordinate and oversee day-to-day operations of multiple research studies in compliance with study protocols and regulatory requirements.
• Screen, recruit, and consent study participants; ensure proper documentation and eligibility assessment.
• Meet with site managers and providers to explain study eligibility
• Collect, process, and manage clinical and research data accurately and in a timely manner.
• Maintain and organize essential regulatory documents, case report forms, and study files.
• Monitor study progress, perform regular audits, and ensure data integrity and protocol compliance.
• Act as a liaison between investigators and research staff.
• Coordinate study visits, procedures, and follow-up schedules for participants.
• Assist with writing reports, abstracts, and manuscripts for publication or presentation.
• Train new staff or students in research procedures and compliance standards.

Qualifications:

Required:

• Travel to Cahaba's rural clinics in Perry, Wilcox counties is required

• Based in-person in Centreville
• Broad Clinical knowledge required
• Ability to manage multiple priorities in a fast-paced environment.
• Strong organizational, interpersonal, and communication skills.
• Demonstrates a high level of initiative and independence in daily tasks

Cahaba Medical Care is an Equal Opportunity Employer.