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.
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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
Office of Clinical Research (OCR) is seeking an experienced, highly organized Multi-Site Clinical Trial Manager (CTM) to oversee the execution of our complex, multi-center clinical trials. In this role, you will serve as the operational backbone of our studies, managing trial progression across multiple clinical research sites from study startup through study close out. The ideal candidate brings a strong background in clinical research, site startup and management, monitoring oversight, and cross-functional leadership, ensuring all milestones are met on time, within budget, and in strict compliance with ICH-GCP guidelines and regulatory requirements. Exceptional people management skills and trouble-shooting skills are required.
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
Learn more about these and other UTSW employee benefits!
EXPERIENCE AND EDUCATION
Required
Education
Master's Degree In science, social science, healthcare administration, or a related field
Experience
5 years Of experience managing clinical trials and
Equivalent combination of education and relevant experience may be considered in lieu of Master's degree.
JOB DUTIES
Oversees the organizational and operational activities of the Disease-Oriented Teams (DOTs). Develops performance standards and expectation for DOT managers and teams, and periodically assess the attainment of these standards.
Consults with DOT managers and faculty leaders to set performance expectations for research nursing and technical staff managing clinical trials. Works with the members of the team to identify, develop and evaluate key core competencies of clinical research personnel in an effort to tailor training needs.
Maintains peer-level working relationships with faculty and academic departments across UTSW to oversee the conduct of clinical trials. Fulfill duties of DOT managers in their absence.
Oversees the financial and administrative resources available for the management of clinical trials by DOTs, working closely with leadership, staff and faculty from various departments with UTSW Medical Center. Develops budget, fee, cost recovery and revenue recommendations for DOT functions. Works with DOT Managers to analyze and review study budgets to ensure that all studies are fiscally sound and that all study costs are recovered or minimized.
Develops and implements best practices for DOT compliance and assurance. Develop and manage all DOT internal monitoring programs to ensure compliance with all relevant rules, regulations and policies.
Coordinates and oversees the management affiliate networks conducting clinical trials. Analyzes and makes recommendations regarding internal process improvements related to optimal time-to-protocol activation.
Leads a committee comprised of faculty and staff to annually review and develop new Standard Operating Procedures (SOPs); recommends new and drafts updates to existing SOPs as necessary.
Directs and oversees the processes for ensuring timely and accurate electronic data capture (EDC) for investigator-initiated clinical trials (IITs). Maintains high-level expertise in EDC for IITs, and implement training and education for managers and staff performing these functions.
Oversees and optimizes the process for collecting, storing and tracking clinical biospecimens, working closing with institutional resources. Ensures storage space is available and managed appropriately.
Performs other duties as assigned.
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 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
Office of Clinical Research (OCR) is seeking an experienced, highly organized Multi-Site Clinical Trial Manager (CTM) to oversee the execution of our complex, multi-center clinical trials. In this role, you will serve as the operational backbone of our studies, managing trial progression across multiple clinical research sites from study startup through study close out. The ideal candidate brings a strong background in clinical research, site startup and management, monitoring oversight, and cross-functional leadership, ensuring all milestones are met on time, within budget, and in strict compliance with ICH-GCP guidelines and regulatory requirements. Exceptional people management skills and trouble-shooting skills are required.
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
Learn more about these and other UTSW employee benefits!
EXPERIENCE AND EDUCATION
Required
Education
Master's Degree In science, social science, healthcare administration, or a related field
Experience
5 years Of experience managing clinical trials and
Equivalent combination of education and relevant experience may be considered in lieu of Master's degree.
JOB DUTIES
Oversees the organizational and operational activities of the Disease-Oriented Teams (DOTs). Develops performance standards and expectation for DOT managers and teams, and periodically assess the attainment of these standards.
Consults with DOT managers and faculty leaders to set performance expectations for research nursing and technical staff managing clinical trials. Works with the members of the team to identify, develop and evaluate key core competencies of clinical research personnel in an effort to tailor training needs.
Maintains peer-level working relationships with faculty and academic departments across UTSW to oversee the conduct of clinical trials. Fulfill duties of DOT managers in their absence.
Oversees the financial and administrative resources available for the management of clinical trials by DOTs, working closely with leadership, staff and faculty from various departments with UTSW Medical Center. Develops budget, fee, cost recovery and revenue recommendations for DOT functions. Works with DOT Managers to analyze and review study budgets to ensure that all studies are fiscally sound and that all study costs are recovered or minimized.
Develops and implements best practices for DOT compliance and assurance. Develop and manage all DOT internal monitoring programs to ensure compliance with all relevant rules, regulations and policies.
Coordinates and oversees the management affiliate networks conducting clinical trials. Analyzes and makes recommendations regarding internal process improvements related to optimal time-to-protocol activation.
Leads a committee comprised of faculty and staff to annually review and develop new Standard Operating Procedures (SOPs); recommends new and drafts updates to existing SOPs as necessary.
Directs and oversees the processes for ensuring timely and accurate electronic data capture (EDC) for investigator-initiated clinical trials (IITs). Maintains high-level expertise in EDC for IITs, and implement training and education for managers and staff performing these functions.
Oversees and optimizes the process for collecting, storing and tracking clinical biospecimens, working closing with institutional resources. Ensures storage space is available and managed appropriately.
Performs other duties as assigned.
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 169+ Clinical Research Jobs in Texas
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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
- Houston Methodist15
- UT Southwestern Medical Center12
- Pinnacle Clinical Research9
- Iterative Health7
- Retina Consultants of Texas7
Top Industries Hiring
- Education10
- Healthcare & Medical Services9
- Science & Research3
- Agriculture & Farming3
- Medical Devices2
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 Houston Methodist, UT Southwestern Medical Center, and Pinnacle Clinical Research, based on current listings on Migrate Mate as of August 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?
Houston, Dallas, and Austin 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 16% of clinical research openings tied to Texas are remote or hybrid as of August 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 169+ Clinical Research Jobs in Texas
Find roles in Texas that match your experience and apply in just a few clicks.
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