Clinical Research Associate Visa Sponsorship Jobs in Texas
Texas is one of the most active states for clinical research associate hiring, with major pharmaceutical and medical device employers concentrated in Houston's Texas Medical Center, the Dallas-Fort Worth Metroplex, and San Antonio. Organizations like MD Anderson Cancer Center, Covance, PPD, and ICON regularly hire CRAs and have established records of visa sponsorship for qualified candidates.
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Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
Join Us as an Associate Clinical Research Manager - Make an Impact at the Forefront of Innovation
The Associate Clinical Research Manager assists with managing various aspects of assigned clinical trials involving patient and healthy subject populations in both inpatient and outpatient settings. Additionally, the Associate Clinical Research Manager acts as liaison between senior project team members and study subjects. The role involves actively participating and assisting with sponsor, investigator and research team communications.
What You'll Do:
- Actively participate with senior project team members to meet project needs, projections and deadlines.
- Oversee organization and accuracy of project documents.
- Work with management on understanding departmental needs and improving processes.
- Provide support for the study conduct, working directly with study monitor and study subjects.
- Oversee data entry, source data QC, EDC data entry and EDC query resolution, lab data verification, subject eligibility status review and subject eligibility notification.
Education & Experience Requirements:
- Bachelor's degree or equivalent and relevant formal academic / vocational qualification
- Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 2 years).
Years of experience refers to typical years of related experience needed to gain the required knowledge, skills, and abilities necessary to perform the essential functions of the job. Years of experience are not to be used as the only determining factor in establishing the job class or making employment selection decisions.
Knowledge, Skills, Abilities:
- Basic knowledge of Phase I processes and clinical study operations
- Fundamental knowledge of FDA regulations and ICH GCP guidelines
- Basic computer skills with working knowledge of Microsoft Office applications
- Time management and multi-tasking skills
- Written and verbal communication skills
- Ability to prioritize workload and adapt to changing study needs
- Ability to act as a liaison between external and internal groups.
Working Conditions and Environment:
- Work is performed in an office/laboratory and/or a clinical environment.
- Exposure to biological fluids with potential exposure to infectious organisms.
- Exposure to electrical office equipment.
- Personal protective equipment required such as protective eyewear, garments and gloves.
Why Join Us?
When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.
Apply today to help us deliver tomorrow’s breakthroughs.
Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
Join Us as an Associate Clinical Research Manager - Make an Impact at the Forefront of Innovation
The Associate Clinical Research Manager assists with managing various aspects of assigned clinical trials involving patient and healthy subject populations in both inpatient and outpatient settings. Additionally, the Associate Clinical Research Manager acts as liaison between senior project team members and study subjects. The role involves actively participating and assisting with sponsor, investigator and research team communications.
What You'll Do:
- Actively participate with senior project team members to meet project needs, projections and deadlines.
- Oversee organization and accuracy of project documents.
- Work with management on understanding departmental needs and improving processes.
- Provide support for the study conduct, working directly with study monitor and study subjects.
- Oversee data entry, source data QC, EDC data entry and EDC query resolution, lab data verification, subject eligibility status review and subject eligibility notification.
Education & Experience Requirements:
- Bachelor's degree or equivalent and relevant formal academic / vocational qualification
- Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 2 years).
Years of experience refers to typical years of related experience needed to gain the required knowledge, skills, and abilities necessary to perform the essential functions of the job. Years of experience are not to be used as the only determining factor in establishing the job class or making employment selection decisions.
Knowledge, Skills, Abilities:
- Basic knowledge of Phase I processes and clinical study operations
- Fundamental knowledge of FDA regulations and ICH GCP guidelines
- Basic computer skills with working knowledge of Microsoft Office applications
- Time management and multi-tasking skills
- Written and verbal communication skills
- Ability to prioritize workload and adapt to changing study needs
- Ability to act as a liaison between external and internal groups.
Working Conditions and Environment:
- Work is performed in an office/laboratory and/or a clinical environment.
- Exposure to biological fluids with potential exposure to infectious organisms.
- Exposure to electrical office equipment.
- Personal protective equipment required such as protective eyewear, garments and gloves.
Why Join Us?
When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.
Apply today to help us deliver tomorrow’s breakthroughs.
Clinical Research Associate Job Roles in Texas
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Search Clinical Research Associate Jobs in TexasClinical Research Associate Jobs in Texas: Frequently Asked Questions
Which companies sponsor visas for clinical research associates in Texas?
Several large contract research organizations and health systems in Texas have sponsored visas for clinical research associates, including PPD (now Thermo Fisher Scientific), ICON plc, Covance, Labcorp Drug Development, and MD Anderson Cancer Center. Large pharmaceutical companies with Texas operations, such as AstraZeneca and Novartis, have also filed H-1B visa petitions for CRA roles. Sponsorship availability varies by position, so confirming with each employer's HR team is worthwhile.
Which visa types are most common for clinical research associate roles in Texas?
The H-1B is the most common visa category for clinical research associates in Texas because the role typically requires at least a bachelor's degree in a life science or related field, meeting the specialty occupation standard. Candidates already authorized under F-1 OPT or STEM OPT extensions often transition to H-1B sponsorship once employed. The TN visa is an option for Canadian and Mexican nationals whose CRA role qualifies under NAFTA/USMCA occupation categories.
Which cities in Texas have the most clinical research associate sponsorship jobs?
Houston leads the state for CRA sponsorship activity, driven by the Texas Medical Center, one of the largest medical complexes in the world, which hosts numerous clinical trial sites and sponsors. Dallas-Fort Worth is the second major hub, with CRO regional offices and hospital networks conducting sponsored trials. San Antonio has a growing presence through the South Texas Medical Center and military-affiliated research institutions such as the Brooke Army Medical Center.
How to find clinical research associate visa sponsorship jobs in Texas?
Migrate Mate is a job board built specifically for international candidates seeking visa sponsorship in the U.S. You can filter directly for clinical research associate roles in Texas to see employers who have a documented history of sponsoring work visas. This saves significant time compared to manually screening job postings, since Migrate Mate focuses exclusively on sponsorship-eligible positions rather than general listings.
Are there state-specific factors that affect CRA visa sponsorship hiring in Texas?
Texas has no state income tax, which influences how employers structure compensation packages and prevailing wage calculations under the H-1B Labor Condition Application process. The concentration of top-tier research universities, including UT Southwestern, Baylor College of Medicine, and UT Health San Antonio, creates a steady pipeline of candidates and established relationships with CROs. Employers at Texas Medical Center sites often have dedicated immigration support teams due to the high volume of international clinical staff they hire.
What is the prevailing wage for sponsored clinical research associate jobs in Texas?
U.S. employers sponsoring a visa must pay at least the prevailing wage, which is what workers in the same role, area, and experience level typically earn. The Department of Labor sets this rate to make sure companies aren't hiring foreign workers simply because they'd accept lower pay than a U.S. worker. It varies by job title, location, and experience. You can look up current prevailing wage rates for any occupation and location using the OFLC Wage Search page.