Clinical Research Jobs in Texas
Clinical Research jobs in Texas are in high demand, concentrated in the pharmaceutical, medical device, and academic medical center sectors, with openings ranging from entry-level clinical research coordinators through senior principal investigators and site directors. Houston, Dallas, and San Antonio are the primary hiring metros, anchored by institutions and employers such as MD Anderson Cancer Center, Baylor Scott and White Health, and ICON plc, which maintain large clinical operations across the state. The most sought-after specialties in Texas include oncology trials, cardiovascular research, and early-phase studies tied to the state's dense network of academic health systems and biotech corridors. Find a role that fits below and apply directly.
Find Clinical Research JobsOverview
Showing 5 of 190+ Clinical Research jobs
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 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.
BENEFITS
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% 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
EXPERIENCE AND EDUCATION
Required
- 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 is in good working order.
- With adequate training and supervision, assists with collecting and processing specimens following established procedures/protocols.
- Assists in preparing studies for closeout, (e.g. packing files, documenting files for storage, shipping extra supplies back to sponsor).
- With adequate training/credentialing and supervision, performs study procedures such as phlebotomy, vital signs, and EKG’s needed for research study. Based on research study, other procedures/equipment/services may be required.
- May perform patient care (basic skills) under the direction of PI following scope of work document.
- Duties performed may include one or more of the following core functions: a) Directly interacting with or caring for patients; b) Directly interacting with or caring for human-subjects research participants; c) Regularly maintaining, modifying, releasing or similarly affecting patient records (including patient financial records); or d) Regularly maintaining, modifying, releasing or similarly affecting human-subjects research records.
- Performs other duties as assigned.
- Knowledge of applicable Federal and institutional regulations governing clinical research.
- Knowledge of clinical research protocols.
- Effective organizational skills and attention to detail.
- Proactively works to maximize results of the team and organization.
- Follows and understands the regulations for Protected Health Information (PHI).
- Proactively works to maximize results of the team and organization.
- Possess strong computer skills (spreadsheets, databases, and interactive web-based software).
- Possess good communication skills.
- Possess the ability to problem solve.
- Work requires ability to conduct interviews with research subjects.
- Clinical Setting
- Office Setting
Salary Information
Salary is commensurate with education, skills, and relevant experience.
SECURITY AND EEO STATEMENT
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.
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 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.
BENEFITS
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% 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
EXPERIENCE AND EDUCATION
Required
- 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 is in good working order.
- With adequate training and supervision, assists with collecting and processing specimens following established procedures/protocols.
- Assists in preparing studies for closeout, (e.g. packing files, documenting files for storage, shipping extra supplies back to sponsor).
- With adequate training/credentialing and supervision, performs study procedures such as phlebotomy, vital signs, and EKG’s needed for research study. Based on research study, other procedures/equipment/services may be required.
- May perform patient care (basic skills) under the direction of PI following scope of work document.
- Duties performed may include one or more of the following core functions: a) Directly interacting with or caring for patients; b) Directly interacting with or caring for human-subjects research participants; c) Regularly maintaining, modifying, releasing or similarly affecting patient records (including patient financial records); or d) Regularly maintaining, modifying, releasing or similarly affecting human-subjects research records.
- Performs other duties as assigned.
- Knowledge of applicable Federal and institutional regulations governing clinical research.
- Knowledge of clinical research protocols.
- Effective organizational skills and attention to detail.
- Proactively works to maximize results of the team and organization.
- Follows and understands the regulations for Protected Health Information (PHI).
- Proactively works to maximize results of the team and organization.
- Possess strong computer skills (spreadsheets, databases, and interactive web-based software).
- Possess good communication skills.
- Possess the ability to problem solve.
- Work requires ability to conduct interviews with research subjects.
- Clinical Setting
- Office Setting
Salary Information
Salary is commensurate with education, skills, and relevant experience.
SECURITY AND EEO STATEMENT
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.
See All 190+ Clinical Research Jobs in Texas
Find roles in Texas that match your experience and apply in just a few clicks.
Find Clinical Research JobsClinical Research Jobs by City in Texas
Where Texas roles are concentrated, by current openings.
Clinical Research Job Market in Texas
A snapshot from current Texas openings, updated as new roles post.
Who's Hiring
- UT Southwestern Medical Center17
- Iterative Health15
- UT Health Science Center at San Antonio8
- Fortrea6
- Houston Methodist6
Top Industries Hiring
- Education11
- Healthcare & Medical Services8
- Science & Research3
- Biotechnology & Pharmaceuticals2
- Agriculture & Farming1
What Texas Employers Look For
The qualifications that appear most often in clinical research jobs across Texas.
- ACRP or SOCRA certification (CCRC, CCRP) recognized by Texas clinical research employers
- Bachelor's degree in life sciences, nursing, or a related healthcare field
- Demonstrated experience with FDA regulations, GCP guidelines, and ICH standards
- Proficiency with electronic data capture systems such as Medidata Rave or REDCap
- Strong background in informed consent processes, protocol deviation reporting, and IRB submissions
- Ability to coordinate multi-site trials within large Texas health systems or CRO environments
Clinical Research Jobs in Texas: Frequently Asked Questions
How do you become a clinical research in Texas?
Most clinical research roles in Texas require at least a bachelor's degree in a life science, nursing, or health-related field, followed by obtaining a nationally recognized credential such as the Certified Clinical Research Coordinator credential from ACRP or the CCRP from SOCRA. Texas does not issue a state-specific clinical research license, so employers rely heavily on these certifications alongside demonstrated GCP training. Entry-level candidates typically start as clinical research assistants or coordinators at a Texas academic medical center or contract research organization before advancing.
Which companies hire clinical researchs in Texas?
Employers hiring clinical researchs in Texas right now include UT Southwestern Medical Center, Iterative Health, and UT Health Science Center at San Antonio, based on current listings on Migrate Mate as of October 2026. Texas's concentration of major health systems, cancer centers, and global CROs creates consistent year-round demand across the state's largest metro areas.
Which Texas cities have the most clinical research jobs?
Dallas, Houston, and San Antonio have the most clinical research openings in Texas. Houston leads because of its dense cluster of cancer centers, academic medical institutions, and life science companies, while Dallas and San Antonio draw significant hiring from large integrated health systems and CRO offices that coordinate multi-site trials throughout the state.
Are there remote clinical research jobs in Texas?
Yes, but they are uncommon for most clinical research roles because the work typically requires on-site patient interaction, specimen handling, and direct trial oversight. About 29% of clinical research openings tied to Texas are remote or hybrid as of October 2026, reflecting the hands-on nature of most positions. The portions most likely to be remote include regulatory affairs coordination, data management, and sponsor-facing project management for experienced coordinators or monitors.
How can I get hired as a clinical research in Texas with little or no experience?
The most realistic entry path is applying for a clinical research assistant or coordinator-in-training role at a large Texas academic medical center such as those affiliated with UT Health, Texas A&M Health, or the Baylor College of Medicine system, which regularly onboard candidates without direct trial experience. Completing a GCP certification course and a research ethics training program strengthens an application considerably. Candidates with backgrounds in phlebotomy, medical assisting, or healthcare administration often transition successfully into entry-level coordinator positions at CROs or community research sites across Houston and Dallas.
Where can I find and apply to clinical research jobs in Texas?
You can find and apply to clinical research jobs in Texas on Migrate Mate, which lists current openings from employers hiring across the state right now. Search the available roles, find the ones that fit your experience and location, and apply directly through each listing.
See All 190+ Clinical Research Jobs in Texas
Find roles in Texas that match your experience and apply in just a few clicks.
Find Clinical Research Jobs