Pediatrics Neurology Research Coordinator II

University of Texas Southwestern Medical Center; Dallas (TX); On-site; USD 60,000 - 80,000; Full time

Job summary

University of Texas Southwestern Medical Center in Dallas seeks a Clinical Research Coordinator II in the Department of Pediatrics, supporting the Neurology division. You will coordinate patient recruitment, consent, data collection, and regulatory management across multiple studies, under supervision of Investigators.

You may assist with budget, policy development, and data management in complex trials, collaborating with a multi-disciplinary team to ensure compliance and study success.

Qualifications

• Education: Bachelor's Degree in medical or science related field.
• Experience: 2 years clinical research experience.
• Preferred: CPR/CPRAED/ACRP or SOCRA certification is a plus.

Responsibilities

• Interact with clinical research participants via telephone, telehealth or in-person.
• Coordinate regulatory documentation for studies to comply with FDA, University policies and hospital policies.
• Schedule procedures per study protocol and assist with consent processes as needed.
• Screen, recruit, enroll and follow subjects according to protocol guidelines.
• Develop and maintain data collection tools and case report forms as required.
• Assist in developing research protocols and writing clinical research protocols.
• Monitor patient safety and ensure reporting per HRPP standards.
• May assist PI with fiscal management and budget preparation.
• Prepare IRB submissions and amendments; coordinate annual reports for regulators.

Education

Bachelor's Degree in medical or science related field

Job description

University of Texas Southwestern Medical Center in Dallas seeks a Clinical Research Coordinator II in the Department of Pediatrics, supporting the Neurology division. You will coordinate patient recruitment, consent, data collection, and regulatory management across multiple studies, under supervision of Investigators.

You may assist with budget, policy development, and data management in complex trials, collaborating with a multi-disciplinary team to ensure compliance and study success.