Trauma Clinical Research Assistant II - Data & Trials

University of Texas Southwestern Medical Center; Dallas (TX); On-site; USD 60,000 - 90,000; Full time

Benefits offered by this job

PPO medical plan

Paid Time Off

Tuition Reimbursement

Parental Leave

Wellness programs

Job summary

UT Southwestern Medical Center is seeking a Clinical Research Data Specialist to support trauma-focused trials. You will manage study databases, track participant visits, and prepare data summaries for measurement-based care.

The role involves data entry, regulatory documentation, and collaboration with the PI and research team to ensure protocol compliance. Training will include consent procedures and potential phlebotomy tasks as needed.

Qualifications

• Education requirements: High School Diploma or Associate's Degree or Bachelor's Degree in medical/science field.
• Experience: 2 years with High School Diploma or 1 year with Associate's Degree.
• Licenses/Certifications may include BLS/CPR AED depending on location requirements.

Responsibilities

• Manage study databases and track participant visits for quality data.
• Prepare weekly patient data summaries for measurement-based care.
• Enter data and maintain regulatory documentation with accuracy.
• Assist with regulatory submissions and IRB communications.
• Recruit and enroll patients under supervision for research studies.
• Conduct consent processes and ensure protocol compliance.

Skills

Data management

Clinical research coordination

Regulatory documentation

QA/QC data checks

Participant recruitment

Education

High School Diploma

Associate's Degree (medical/science)

Bachelor's Degree (medical/science)

Tools

Data entry systems

IRB familiarity

Job description

UT Southwestern Medical Center is seeking a Clinical Research Data Specialist to support trauma-focused trials. You will manage study databases, track participant visits, and prepare data summaries for measurement-based care.

The role involves data entry, regulatory documentation, and collaboration with the PI and research team to ensure protocol compliance. Training will include consent procedures and potential phlebotomy tasks as needed.