Clinical Trials Coordinator II - Patient-Centric Research

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

Benefits offered by this job

Healthcare benefits

Paid time off

On-site childcare

Wage merit increases

Paid holidays

Job summary

UT Southwestern Medical Center in Dallas, TX seeks a Clinical Research Coordinator II to coordinate research projects within the Internal Medicine CTU. You will manage patient recruitment, screening, and enrollment, and oversee data management for multiple studies.

You will ensure regulatory compliance, prepare IRB submissions, and collaborate with investigators across Cardiology and Hematology. A Bachelor's degree and 2 years of clinical research experience are required; CCRA or CPR

Qualifications

• Bachelor's Degree in medical or science related field.
• 2 years clinical research experience.
• ACRP or SOCRA certification a plus.
• BLS/CPR may be required based on study protocols or location.

Responsibilities

• Direct interaction with clinical research participants via telephone, telehealth or in-person.
• Coordinate regulatory documentation to comply with FDA, policies and IRB requirements.
• Screen, recruit, enroll and follow subjects per protocol guidelines.
• Develop and manage data collection tools and CRFs for studies.
• Assist in developing research protocols and provide training to team members.

Education

Bachelor's Degree in medical or science related field

Job description

UT Southwestern Medical Center in Dallas, TX seeks a Clinical Research Coordinator II to coordinate research projects within the Internal Medicine CTU. You will manage patient recruitment, screening, and enrollment, and oversee data management for multiple studies.

You will ensure regulatory compliance, prepare IRB submissions, and collaborate with investigators across Cardiology and Hematology. A Bachelor's degree and 2 years of clinical research experience are required; CCRA or CPR