Clinical Research Coordinator I — Patient-Focused Trials

UT Southwestern Medical Center; Dallas (TX); On-site; USD 64,000 - 90,000; Full time

Benefits offered by this job

PPO health plan

Paid time off

Parental leave

TRS retirement

Wellness programs

Tuition reimbursement

PSLF eligible

Job summary

UT Southwestern Medical Center in Dallas seeks a Research Coordinator to support both clinical and basic research projects. You will coordinate patient visits, data collection, sample handling, and quality control under investigator supervision.

The ideal candidate has 1 year of clinical research experience, strong communication, and RedCap familiarity. Phlebotomy skills and IRB exposure are a plus; proficiency with Microsoft Office is required.

Qualifications

• Education at least a Bachelor's degree in medical or science field.
• 1 year of clinical research experience preferred; more with advanced degree may be considered.
• Experience with RedCap is preferred.
• Phlebotomy experience is desirable.
• Strong communication and organizational skills required.

Responsibilities

• Direct interaction with clinical research participants via in-person, phone, or telehealth.
• Coordinate regulatory aspects and ensure compliance with policies and FDA requirements.
• Schedule study procedures and manage protocol logistics with oversight from the PI.
• Screen, recruit, enroll, and follow subjects per protocol guidelines.
• Maintain data collection tools (CRFs) and assist with protocol development and budgeting.

Skills

Clinical research experience

Interdisciplinary teamwork

Communication skills

Phlebotomy experience

RedCap experience

Strong organizational skills

Education

Bachelor's Degree or higher in medical or science related field

Tools

RedCap

Microsoft Office Suite

Job description

UT Southwestern Medical Center in Dallas seeks a Research Coordinator to support both clinical and basic research projects. You will coordinate patient visits, data collection, sample handling, and quality control under investigator supervision.

The ideal candidate has 1 year of clinical research experience, strong communication, and RedCap familiarity. Phlebotomy skills and IRB exposure are a plus; proficiency with Microsoft Office is required.