More jobs:
Clinical Research Coordinator , Lab Trivedi
Job in
Dallas, Dallas County, Texas, 75202, USA
Listed on 2026-10-09
Listing for:
UT Southwestern
Full Time
position Listed on 2026-10-09
Job specializations:
-
Healthcare
Clinical Research
Job Description & How to Apply Below
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 No. 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 Works under the direction of an Investigator(s) with general supervision, to coordinate research projects. This position primarily performs patient/participant coordination, however, may conduct data management in smaller departments on as needed basis.
Collects and ensures quality control of clinical or basic research data in support of multiple and/or complex research studies. The preferred candidate would possess the following qualifications/skills:
Experience in both clinical and research study settings
Ability to work within an interdisciplinary team Strong written and oral communication skills
Experience with Microsoft Office Suite Strong organizational skills
Among other activities, the position will be responsible for:
Direct interaction with clinical research participants enrolled in RAD/D2K (and possibly to include other studies)
Coordination of study procedures, activities, and payments
Collection of longitudinal study data and ensuring quality control of clinical research data Overseeing patient retention
Supporting IRB maintenance and drafting of manuscripts and/or funding proposals
May be involved in sample collecting and processing
The ideal candidate will have a minimum of 2 years of experience working directly with participants/patients in clinical research studies. S/he will also be able to perform phlebotomy and have experience working with human tissue (including plasma, serum, and urine) specimens. Finally, experience working in Redcap is preferred. BENEFITSUT Southwestern is proud to offer a competitive and comprehensive benefits package to eligible employees.
Our benefits are designed to support your overall wellbeing, and include:
PPO medical plan, available day one at no cost for full-time employee-only coverage
100% coverage for preventive healthcare-no copay
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 Learn more about these and other UTSW employee benefits!
EXPERIENCE AND EDUCATION Required Education Bachelor 's Degree or higher degree in medical or science related field Experience1 year of clinical research experience May consider additional years of experience or advanced degree in lieu of education or experience, respectively. Preferred Licenses and Certifications(BLS) BASIC LIFE SUPPORT Licensure may be required based on research study protocols or affiliate location requirements. (CPRAED) CPR AED Licensure may be required based on research study protocols or affiliate location requirements.
ACRP or SOCRA certification a plus JOB DUTIES Directly interacts with clinical research participants, as required, for the research study. Interacts via telephone, telehealth or in-person.
Coordinate regulatory aspects of the trial including maintaining and developing regulatory information to comply with industry…
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