ObGyn Clinical Research Assistant II — Data & Trials

The University of Texas Southwestern Medical Center; Dallas (TX); On-site; USD 45,000 - 65,000; Full time

Benefits offered by this job

PPO medical plan

Preventive care coverage

Paid Time Off

TRS retirement programs

Paid parental leave

Wellness programs

Tuition reimbursement

PSLF-qualified employer

Job summary

UT Southwestern Medical Center in Dallas seeks a Clinical Research Assistant II to support multiple clinical studies under supervision. Responsibilities include recruiting, screening, enrolling, coordinating visits, and handling data via CRFs, EPIC, and QA/QC to ensure protocol adherence.

The role collaborates with investigators, coordinators, and nurses, supporting start-up, maintenance, and closeout activities, and assisting with regulatory submissions while maintaining data integrity.

Qualifications

• Education and experience requirements as stated in the job posting.
• Ability to perform data entry, manage visits, and maintain study records.

Responsibilities

• Supports multiple clinical studies under supervision.
• Recruits, screens, consents, enrolls participants and coordinates visits.
• Explains study procedures and collects data via CRFs and EPIC.
• Performs data quality reviews and resolves queries.
• Assists with regulatory documentation and IRB-related tasks.
• Maintains databases and data integrity for study files.
• May assist with biospecimen handling and shipping.
• Supports study start-up, maintenance, and closeout activities.

Education

Education: High School Diploma or Associate's Degree or Bachelor's Degree in medical/science

Experience: 2 years with HS Diploma or 1 year with AA

Job description

UT Southwestern Medical Center in Dallas seeks a Clinical Research Assistant II to support multiple clinical studies under supervision. Responsibilities include recruiting, screening, enrolling, coordinating visits, and handling data via CRFs, EPIC, and QA/QC to ensure protocol adherence.

The role collaborates with investigators, coordinators, and nurses, supporting start-up, maintenance, and closeout activities, and assisting with regulatory submissions while maintaining data integrity.