Clinical Research Assistant II: Data & Trials

UT Southwestern Medical Center

Dallas (TX)

On-site

USD 52,000 - 82,000

Full time

6 days ago
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Benefits offered by this job

PPO health plan
Paid time off
TRS retirement
Parental leave
Wellness programs
Tuition reimbursement
PSLF eligibility

Job summary

UT Southwestern Medical Center is seeking a data management professional to support local and national research studies. The role involves coordinating observational trials, maintaining data integrity, and assisting with regulatory documentation under supervision.

Responsibilities include data entry, eligibility screening, and preparation of study records. A background in medical or science fields and some clinical research experience are preferred.

Qualifications

  • Experience in data entry and data integrity checks.
  • Familiarity with clinical research processes and study protocols.
  • Ability to review records and abstract information for studies.

Responsibilities

  • Understand visit schedules, criteria and protocol requirements for trials.
  • Assist research staff with protocol related tasks and data entry.
  • Review medical records for eligibility criteria.
  • Enter data into case report forms and maintain study documentation.
  • Support data queries, audits, and regulatory submissions.
  • Maintain databases and ensure data integrity.
  • Assist with QA/QC checks and study closeout activities.
  • Support recruitment and consent processes under supervision.

Skills

Data management
Research coordination

Education

High School Diploma
Associate's Degree in medical or science related field
Bachelor's Degree in medical or science related field

Job description

UT Southwestern Medical Center is seeking a data management professional to support local and national research studies. The role involves coordinating observational trials, maintaining data integrity, and assisting with regulatory documentation under supervision.

Responsibilities include data entry, eligibility screening, and preparation of study records. A background in medical or science fields and some clinical research experience are preferred.

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