Clinical Research Coordinator

Job Summary

To support a groundbreaking clinical trial, the full-time Clinical Research Coordinator will manage participant recruitment, coordinate study logistics, and maintain data records in compliance with Good Clinical Practices, working onsite in Austin, Texas.

Key responsibilities

• Coordinate protocol-related research procedures, ensuring compliance with IRB-approved protocols and Good Clinical Practices
• Participate in all study components, including case management, data collection, and participant experience enhancement
• Manage communication with research participants and stakeholders, ensuring accurate data entry and follow-up assessments

Required qualifications

• Familiarity with research studies and tabular data is preferred; no specific degree required
• Prior laboratory or human subjects research experience
• Strong interest in clinical research
• Professional demeanor when interacting with participants
• Strong organizational and interpersonal skills