Clinical Research Data Coordinator I

University of Texas Southwestern Medical Center; Dallas (TX); On-site; USD 50,000 - 70,000; Full time

Benefits offered by this job

PPO medical plan day one

Paid Time Off

Retirement Programs through TRS

Paid Parental Leave Benefit

Wellness programs

Tuition Reimbursement

Public Service Loan Forgiveness (PSLF)

UT Southwestern employee benefits

Job summary

UT Southwestern Medical Center in Dallas seeks a data management support member for ongoing local and national research studies. The role emphasizes data entry, study coordination, and ensuring data integrity while supporting regulatory submissions and documentation.

Responsibilities include handling case report forms, data queries, and preparing reports for IRB and sponsor requirements, with adherence to protocol timelines and safety standards.

Qualifications

• High School Diploma or GED required.
• Prior experience with data entry and data management preferred.
• Familiarity with regulatory requirements and IRB processes advantageous.

Responsibilities

• Enter data into case report forms or data collection systems.
• Assist with data queries and edits for accuracy.
• Compile data for regulatory requirements and sponsor submissions.
• Maintain existing databases and ensure data integrity.
• Understand visit schedules, criteria and protocol requirements for routine trials.
• Assist research staff with protocol-related tasks.
• Prepare annual reports or IRB modifications as needed.
• Recruit and enroll patients in research studies when appropriate.
• Order and maintain research supplies; ensure equipment is in good working order.
• Collect and process specimens following established procedures.

Skills

Data entry

Attention to detail

Study coordination

Education

High School Diploma or GED

BLS CPR AED (Preferred)

Job description

UT Southwestern Medical Center in Dallas seeks a data management support member for ongoing local and national research studies. The role emphasizes data entry, study coordination, and ensuring data integrity while supporting regulatory submissions and documentation.

Responsibilities include handling case report forms, data queries, and preparing reports for IRB and sponsor requirements, with adherence to protocol timelines and safety standards.