Clinical Trial Associate Jobs in Texas
Clinical Trial Associate jobs in Texas are active across a strong mix of pharmaceutical, biotechnology, and academic medical research sectors, with openings ranging from entry-level research coordinators to senior clinical operations roles. Houston, Dallas, and San Antonio anchor most of the hiring, where major employers like MD Anderson Cancer Center, PPD (a Thermo Fisher Scientific company), and ICON plc maintain substantial clinical operations teams. The most in-demand specialties include oncology trials, cardiovascular studies, and regulatory document management. Find a role that fits below and apply directly.
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Showing 5 of 110+ Clinical Trial Associate jobs
JOB SUMMARY
Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience related to CNS/Neuroscience for a full-time, office-based Associate Clinical Trial Manager (aCTM) based in our Dallas, TX office. The aCTM is part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management.
This is a fantastic opportunity for recent PhD graduates to enter the industry, receive solid foundational training, work in an international environment, and develop their career in the research and development of cutting-edge therapeutics. Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM).
Responsibilities:
- Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager
- Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy
- Compile and maintain project-specific status reports within the clinical trial management system
- Interact with the internal project team, Sponsor, study sites, and third-party vendors
- Provide oversight and quality control of our internal regulatory filing system
- Provide oversight and management of study supplies
- Create and maintain project timelines
- Coordinate project meetings and produce quality minutes
QUALIFICATIONS
- PhD in Life Sciences
- Expertise related to CNS/Neuroscience
- Ability to work in a fast-paced dynamic industry within an international team
- Prior experience within the CRO or pharmaceutical industry not required but will be advantageous
MEDPACE OVERVIEW:
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 6,000 people across 40+ countries.
WHY MEDPACE?:
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
DALLAS PERKS:
- Flexible work environment
- Competitive PTO packages, starting at 20+ days
- Competitive compensation and benefits package
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives
- Community involvement with nonprofit organizations
- Structured career paths with opportunities for professional growth
- Discounts on local sports games, fitness gyms and attractions
- Modern, ecofriendly campus with an on-site fitness center
- Free on-site parking
- Outdoor seating and workspace
AWARDS:
- Named a Top Workplace in 2024 by The Cincinnati Enquirer
- Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
- Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
WHAT TO EXPECT NEXT
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
JOB SUMMARY
Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience related to CNS/Neuroscience for a full-time, office-based Associate Clinical Trial Manager (aCTM) based in our Dallas, TX office. The aCTM is part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management.
This is a fantastic opportunity for recent PhD graduates to enter the industry, receive solid foundational training, work in an international environment, and develop their career in the research and development of cutting-edge therapeutics. Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM).
Responsibilities:
- Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager
- Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy
- Compile and maintain project-specific status reports within the clinical trial management system
- Interact with the internal project team, Sponsor, study sites, and third-party vendors
- Provide oversight and quality control of our internal regulatory filing system
- Provide oversight and management of study supplies
- Create and maintain project timelines
- Coordinate project meetings and produce quality minutes
QUALIFICATIONS
- PhD in Life Sciences
- Expertise related to CNS/Neuroscience
- Ability to work in a fast-paced dynamic industry within an international team
- Prior experience within the CRO or pharmaceutical industry not required but will be advantageous
MEDPACE OVERVIEW:
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 6,000 people across 40+ countries.
WHY MEDPACE?:
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
DALLAS PERKS:
- Flexible work environment
- Competitive PTO packages, starting at 20+ days
- Competitive compensation and benefits package
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives
- Community involvement with nonprofit organizations
- Structured career paths with opportunities for professional growth
- Discounts on local sports games, fitness gyms and attractions
- Modern, ecofriendly campus with an on-site fitness center
- Free on-site parking
- Outdoor seating and workspace
AWARDS:
- Named a Top Workplace in 2024 by The Cincinnati Enquirer
- Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
- Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
WHAT TO EXPECT NEXT
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
See All 110+ Clinical Trial Associate Jobs in Texas
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Find Clinical Trial Associate JobsClinical Trial Associate Jobs by City in Texas
Where Texas roles are concentrated, by current openings.
Clinical Trial Associate Job Market in Texas
A snapshot from current Texas openings, updated as new roles post.
Who's Hiring
- Baylor College of Medicine22
- Medpace20
- Baylor Scott & White Health6
- The University of Texas at Austin6
- Texas A&M AgriLife Extension5
Top Industries Hiring
- Education63
- Healthcare & Medical Services20
- Science & Research20
- Biotechnology & Pharmaceuticals14
- Agriculture & Farming3
What Texas Employers Look For
The qualifications that appear most often in clinical trial associate jobs across Texas.
- Bachelor's degree in life sciences, nursing, or a related clinical field required
- One to three years of experience in clinical research coordination or trial monitoring preferred
- Familiarity with ICH-GCP guidelines and FDA regulatory requirements for clinical trials
- Proficiency with electronic data capture systems such as Medidata Rave or Oracle Clinical
- Strong document management skills for essential trial files and regulatory binders
- Ability to support site initiation, monitoring visits, and closeout activities independently
Clinical Trial Associate Jobs in Texas: Frequently Asked Questions
How do you become a clinical trial associate in Texas?
Most clinical trial associate positions in Texas require a bachelor's degree in a life science, nursing, or health-related field, followed by entry-level experience in clinical research or a related healthcare setting. Texas does not issue a state-specific license for this role, but employers strongly value the Certified Clinical Research Associate credential offered by the Association of Clinical Research Professionals. Academic medical centers across Houston and Dallas frequently hire candidates who complete clinical research certificate programs at Texas universities.
Which companies hire clinical trial associates in Texas?
Employers hiring clinical trial associates in Texas right now include Baylor College of Medicine, Medpace, and Baylor Scott & White Health, based on current listings on Migrate Mate as of June 2026. Texas's concentration of large academic cancer centers, contract research organizations, and pharmaceutical headquarters makes it one of the more consistent markets for clinical trial staffing in the country.
Which Texas cities have the most clinical trial associate jobs?
Houston, Irving, and Austin account for the most clinical trial associate openings in Texas. Houston leads because of its dense cluster of oncology research institutions and the Texas Medical Center, while Dallas and Austin draw demand from contract research organizations and the growing life sciences corridors in both metros.
Are there remote clinical trial associate jobs in Texas?
Yes, though availability depends heavily on the trial phase and sponsor requirements. About 5% of clinical trial associate openings tied to Texas are remote or hybrid as of June 2026, reflecting the role's mix of site-based and administrative work. Regulatory document review, data reconciliation, and sponsor communication tend to be the most remote-compatible functions, while site monitoring visits remain on-site by nature.
How can I get hired as a clinical trial associate in Texas with little or no experience?
The most realistic entry path is a clinical research coordinator role at a Texas hospital or academic medical center, where hands-on trial experience is built under supervision. The Texas Medical Center in Houston and UT Southwestern Medical Center in Dallas both run research coordinator programs that train candidates without prior clinical trial backgrounds. Lateral moves from roles like clinical data associate, regulatory affairs assistant, or study coordinator give candidates a strong foundation, and completing the ACRP Clinical Research Associate certification before applying gives an edge over other entry-level applicants.
Where can I find and apply to clinical trial associate jobs in Texas?
You can find and apply to clinical trial associate jobs in Texas on Migrate Mate, which lists current openings from employers actively hiring across the state. Search the listings, find roles that match your experience and location, and apply directly to the ones that fit.
See All 110+ Clinical Trial Associate Jobs in Texas
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