Clinical Research Assistant II: Data & Study Coordination

The University of Texas Southwestern Medical Center; Dallas (TX); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

PPO medical plan

100% coverage preventive healthcare

Paid Time Off

TRS retirement programs

Paid parental leave

Wellness programs

Tuition reimbursement

PSLF Qualified Employer

Job summary

UT Southwestern Medical Center in Dallas, TX seeks a Clinical Research Assistant II to support data management for local and national studies under supervision. The role may involve coordinating observational trials and assisting with more complex studies under PI direction.

The successful candidate will help with regulatory documentation, data entry, and quality checks, while potentially contributing to patient recruitment and consent processes in various research projects.

Qualifications

• Education requirements as listed: HS diploma or higher; Associate's or Bachelor's in medical/science field.
• Experience: 2 years with HS or 1 year with Associate degree.

Responsibilities

• Understands visit schedules, criteria and protocol requirements for low complexity trials.
• Assists research staff by completing protocol-related tasks.
• Reviews and abstracts information from medical records for eligibility.
• Enters data into case report forms and maintains study documentation.
• Performs data queries and edits for accuracy and quality checks.
• Prepares regulatory submissions and supports audits.
• Recruits and enrolls patients and conducts consent with supervision.
• Assists with collecting and processing specimens per procedures.

Skills

Data management

Clinical research coordination

Regulatory documentation

IRB knowledge

Education

High School Diploma or equivalent

Associate's Degree in medical or science related field

Bachelor's Degree in medical or science related field

Job description

UT Southwestern Medical Center in Dallas, TX seeks a Clinical Research Assistant II to support data management for local and national studies under supervision. The role may involve coordinating observational trials and assisting with more complex studies under PI direction.

The successful candidate will help with regulatory documentation, data entry, and quality checks, while potentially contributing to patient recruitment and consent processes in various research projects.