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Clinical Research Assistant II, Digestive and Liver

Job in Dallas, Dallas County, Texas, 75215, USA
Listing for: The University of Texas Southwestern Medical Center
Full Time position
Listed on 2026-01-11
Job specializations:
  • Healthcare
    Clinical Research
  • Research/Development
    Clinical Research, Research Assistant/Associate
Job Description & How to Apply Below

Job Description - Clinical Research Assistant II, Digestive and Liver (916444)

Clinical Research Assistant II, Digestive and Liver - ( 916444 )

WHY UT SOUTHWESTERN?

With over 75 years of excellence in Dallas-Fort Worth, Texas, UT Southwestern is committed to excellence, innovation, teamwork, and compassion. As a world-renowned medical and research center, we strive to provide the best possible care, resources, and benefits for our valued employees. Ranked as the number 1 hospital in Dallas-Fort Worth according to U.S. News & World Report, we invest in you with opportunities for career growth and development to align with your future goals.

Our highly competitive benefits package offers healthcare, PTO, and paid holidays, on-site childcare, wage, merit increases and so much more. We invite you to be a part of the UT Southwestern team where you'll discover a culture of teamwork, professionalism, and a rewarding career!

JOB SUMMARY

This position supports Dr. Mack C. Mitchell on his research endeavors. Dr. Mack is Vice President for Medical Affairs at UT Southwestern Medical Center and the Nancy S. and Jeremy L. Professor of Gastroenterology. He is principal investigator for an NIH‑sponsored clinical research study on liver disease related to alcohol and has authored or co‑authored numerous papers and chapters on alcohol and liver diseases. This role works under the direction of an Investigator(s) with general supervision, to provide ongoing data management for local and national research studies and may coordinate observational (non‑treatment/treatment) trials/studies.

May provide supporting role for more complex studies under the direction of the PI, Clinical Research Coordinator and/or Clinical Research Lead.
Bilingual in English and Spanish highly preferred.

BENEFITS
  • PPO medical plan, available day one at no cost for full‑time employee‑only coverage
  • Paid Time Off, available day one
  • Retirement Programs through the Teacher Retirement System of Texas (TRS)
  • Paid Parental Leave Benefit
  • Wellness programs
  • Tuition Reimbursement
  • Public Service Loan Forgiveness (PSLF) Qualified Employer
  • Education
    High School Diploma or
    Associate’s Degree in medical or science related field or
    Bachelor’s Degree medical or science related field and no prior experience
  • Experience
    2 years experience with High School Diploma or
    1 year experience with Associate’s Degree
Preferred
  • Licenses and Certifications
    (BLS) BASIC LIFE SUPPORT may be required based on affiliate location requirements.
    (CPRAED) CPR AED may be required based on affiliate location requirements.
JOB DUTIES
  • Understands visit schedules, criteria and protocol requirements for low complexity trials (e.g., questionnaire, data registry, scripted); schedules research visits.
  • Assists research staff by completing research protocol related tasks.
  • Reviews and abstracts information from medical records including eligibility criteria.
  • Enters data into case report forms or other data collection system based on research study. Assists with maintenance of study level documentation.
  • Assists with data queries and possible edits for accuracy.
  • Compiles data for regulatory requirements and/or deadlines for local or sponsor submissions.
  • Maintains existing databases and ensures data integrity.
  • Performs QA/QC clinical analysis and data checks using various databases based on trial.
  • Assists with preparing annual reports and/or modifications to institutional review board (IRB). This may include reportable events (UPIRSO).
  • Assist and prepare research records for formal sponsor audits or internal audits.
  • Recruits and enrolls patients in research study that may include consenting patients after training and with supervision.
  • With adequate training and supervision, assists with participant screening and recruitment for more complex trials.
  • Conducts and documents consent for participants in studies. Assists with the development of consent plans and documents for participants.
  • Identifies incomplete, inaccurate, or missing data for more complex studies and works with lead coordinator to correct errors.
  • Assists with ordering and maintaining research supplies following university/department procedures, ensuring that equipment…
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