UT Southwestern Medical Center·Dallas, Texas
Coordinates research projects within the Internal Medicine Clinical Trials Unit, focusing on participant recruitment, screening, and enrollment. Manages regulatory documentation, data collection, and ensures compliance with FDA and University policies.
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 Works under the direction of an Investigator(s) with limited 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 Department of Internal Medicine is seeking a Clinical Research Coordinator II to join the Clinical Trials Unit (CTU).
The formation of the CTU is an initiative led by the office of the Internal Medicine Department Chair.
As a valued team member, you will work with clinical trials from various divisions within Internal Medicine including but not limited to Cardiology and Hematology and will manage key aspects of the unit's investigational drug and device clinical trials.
This includes determining effective strategies for recruiting trial participants, screening, consenting, and enrolling participants, and overseeing data management.
UT 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%25 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!
Security This position is security-sensitive and subject to Texas Education Code 51.215, which authorizes UT Southwestern to obtain criminal history record information.
EEO UT Southwestern Medical Center is committed to an educational and working environment that provides equal opportunity to all members of the University community. As an equal opportunity employer, UT Southwestern prohibits unlawful discrimination, including discrimination on the basis of race, color, religion, national origin, sex, sexual orientation, gender identity, gender expression, age, disability, genetic information, citizenship status, or veteran status.
Requires a Bachelor's degree in a medical or science-related field and 2 years of clinical research experience. BLS/CPR certification may be required, and ACRP or SOCRA certification is preferred.
Market context
Clinical Research Coordinator II roles in Texas are often tied to academic medical centers, hospital systems, and research-heavy internal medicine programs, so demand tends to follow active clinical trial pipelines. These positions are competitive because employers usually want a science-related bachelor’s degree, prior clinical research experience, and sometimes BLS/CPR, with ACRP or SOCRA credentials preferred. Before applying, compare the trial area and required certifications, and use the AI-summarized requirements and benefits here to save time reviewing the original posting.
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