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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JOB POSTING TITLE:
Clinical Research Associate I
HIRING DEPARTMENT:
Department of Psychiatry
POSITION OPEN TO:
All Applicants
WEEKLY SCHEDULED HOURS:
40
FLSA STATUS:
Exempt
EARLIEST START DATE:
Apr 20, 2026
POSITION DURATION:
Expected to Continue Until Aug 31, 2027
LOCATION:
UT MAIN CAMPUS
JOB DETAILS:
General Notes
Dell Medical School is seeking a Clinical Research Associate I. This is a grant funded position with an end date of August 31, 2027.
PURPOSE:
The Clinical Research Associate I (CRA I) will conduct interviews and support research project management for two different mental health studies. One study is focused on the impact of a traumatic event on a child’s mental health, and the other study is focused on the cognitive impact of early psychosis on adolescents and young adults who are within two years of their psychotic disorder diagnosis. Key responsibilities include site management, data collection, and ensuring the integrity of clinical data.
Responsibilities:
Site Management
- Ensures compliance with study protocols and regulatory requirements.
- Manages site performance and resolves issues.
Data Collection and Management
- Conducts participant interviews.
- Ensures accurate and timely data entry into electronic data capture systems.
- Reviews and resolves data queries.
Regulatory Compliance
- Ensures adherence to Good Clinical Practice (GCP) and International Council for Harmonisation (ICH) guidelines.
- Facilitates institutional review board (IRB) applications, submissions, and updates across multiple sites.
- Prepares and maintains regulatory documents.
- Coordinates with ethics committees to safeguard participant rights.
Participant Recruitment and Retention
- Coordinates with clinical partners to identify eligible study participants.
- Assists in screening, enrolling, and consenting of study participants.
- Maintains communication with participants to ensure retention.
- Addresses participant concerns and queries.
Reporting and Documentation
- Prepares study reports and documentation.
- Maintains accurate records of study activities.
- Assists in the preparation of manuscripts and publications.
MARGINAL OR PERIODIC FUNCTIONS:
- Conducts literature reviews to support study design and protocol development.
- Assists in the training of new site staff and research team members.
- Participates in internal and external audits.
- Supports the development of study protocols and case report forms.
- Attends conferences and workshops to stay updated on industry trends.
- Adheres to internal controls and reporting structure.
- Performs related duties as required.
KNOWLEDGE/SKILLS/ABILITIES
- Double-checks work for errors, maintains organized records, and follows detailed procedures.
- Writes clear and concise reports, actively listens to others, and presents information effectively.
- Analyzes information, develops solutions, and implements corrective actions.
- Shares information, supports team decisions, and contributes to team success.
- Prioritizes tasks, sets realistic deadlines, and uses time efficiently.
REQUIRED QUALIFICATIONS
Requires a Bachelor's Degree in psychology, social work, public health, or a related field with at least 1 year(s) of experience in clinical research.
Relevant education and experience may be substituted as appropriate.
PREFERRED QUALIFICATIONS
- Master's Degree in psychology, social work, public health, or a related field with at least 2 year(s) of clinical research experience.
- Experience working with children, adolescents and young people who have a mental health condition.
- Fluent in Spanish.
- Certified Clinical Research Associate (CCRA) or Certified Clinical Research Professional (CCRP).
SALARY RANGE
$40,000 + depending on qualifications
WORKING CONDITIONS
- Standard office equipment
- Repetitive use of a keyboard
- Use of manual dexterity.
- Occasional weekends, overtime and evening work to meet deadlines
REQUIRED MATERIALS
- Resume/CV
- 3 work references with their contact information; at least one reference should be from a supervisor
- Letter of interest
Important for applicants who are NOT current university employees or contingent workers: You will be prompted to submit your resume the first time you apply, then you will be provided an option to upload a new Resume for subsequent applications. Any additional Required Materials (letter of interest, references, etc.) will be uploaded in the Application Questions section; you will be able to multi-select additional files. Before submitting your online job application, ensure that ALL Required Materials have been uploaded. Once your job application has been submitted, you cannot make changes.
Important for Current university employees and contingent workers: As a current university employee or contingent worker, you MUST apply within Workday by searching for Find UT Jobs. If you are a current University employee, log-in to Workday, navigate to your Worker Profile, click the Career link in the left hand navigation menu and then update the sections in your Professional Profile before you apply. This information will be pulled in to your application. The application is one page and you will be prompted to upload your resume. In addition, you must respond to the application questions presented to upload any additional Required Materials (letter of interest, references, etc.) that were noted above.
EMPLOYMENT ELIGIBILITY:
Regular staff who have been employed in their current position for the last six continuous months are eligible for openings being recruited for through University-Wide or Open Recruiting, to include both promotional opportunities and lateral transfers. Staff who are promotion/transfer eligible may apply for positions without supervisor approval.
RETIREMENT PLAN ELIGIBILITY:
The retirement plan for this position is Teacher Retirement System of Texas (TRS), subject to the position being at least 20 hours per week and at least 135 days in length.
BACKGROUND CHECKS:
A criminal history background check will be required for finalist(s) under consideration for this position.
EQUAL OPPORTUNITY EMPLOYER:
The University of Texas at Austin, as an equal opportunity/affirmative action employer, complies with all applicable federal and state laws regarding nondiscrimination and affirmative action. The University is committed to a policy of equal opportunity for all persons and does not discriminate on the basis of race, color, national origin, age, marital status, sex, sexual orientation, gender identity, gender expression, disability, religion, or veteran status in employment, educational programs and activities, and admissions.
PAY TRANSPARENCY:
The University of Texas at Austin will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information.
EMPLOYMENT ELIGIBILITY VERIFICATION:
If hired, you will be required to complete the federal Employment Eligibility Verification I-9 form. You will be required to present acceptable and original documents to prove your identity and authorization to work in the United States. Documents need to be presented no later than the third day of employment. Failure to do so will result in loss of employment at the university.
E-VERIFY:
The University of Texas at Austin uses E-Verify to check the work authorization of all new hires effective May 2015. The university’s company ID number for purposes of E-Verify is 854197. For more information about E-Verify, please see the following:
- E-Verify Poster (English and Spanish) [PDF]
- Right to Work Poster (English) [PDF]
- Right to Work Poster (Spanish) [PDF]
COMPLIANCE:
Employees may be required to report violations of law under Title IX and the Jeanne Clery Disclosure of Campus Security Policy and Crime Statistics Act (Clery Act). If this position is identified as a Campus Security Authority (Clery Act), you will be notified and provided resources for reporting. Responsible employees under Title IX are defined and outlined in HOP-3031.
The Clery Act requires all prospective employees to be notified of the availability of the Annual Security and Fire Safety report. You may access the most recent report here or obtain a copy at University Compliance Services, 1616 Guadalupe Street, UTA 2.206, Austin, Texas 78701.

JOB POSTING TITLE:
Clinical Research Associate I
HIRING DEPARTMENT:
Department of Psychiatry
POSITION OPEN TO:
All Applicants
WEEKLY SCHEDULED HOURS:
40
FLSA STATUS:
Exempt
EARLIEST START DATE:
Apr 20, 2026
POSITION DURATION:
Expected to Continue Until Aug 31, 2027
LOCATION:
UT MAIN CAMPUS
JOB DETAILS:
General Notes
Dell Medical School is seeking a Clinical Research Associate I. This is a grant funded position with an end date of August 31, 2027.
PURPOSE:
The Clinical Research Associate I (CRA I) will conduct interviews and support research project management for two different mental health studies. One study is focused on the impact of a traumatic event on a child’s mental health, and the other study is focused on the cognitive impact of early psychosis on adolescents and young adults who are within two years of their psychotic disorder diagnosis. Key responsibilities include site management, data collection, and ensuring the integrity of clinical data.
Responsibilities:
Site Management
- Ensures compliance with study protocols and regulatory requirements.
- Manages site performance and resolves issues.
Data Collection and Management
- Conducts participant interviews.
- Ensures accurate and timely data entry into electronic data capture systems.
- Reviews and resolves data queries.
Regulatory Compliance
- Ensures adherence to Good Clinical Practice (GCP) and International Council for Harmonisation (ICH) guidelines.
- Facilitates institutional review board (IRB) applications, submissions, and updates across multiple sites.
- Prepares and maintains regulatory documents.
- Coordinates with ethics committees to safeguard participant rights.
Participant Recruitment and Retention
- Coordinates with clinical partners to identify eligible study participants.
- Assists in screening, enrolling, and consenting of study participants.
- Maintains communication with participants to ensure retention.
- Addresses participant concerns and queries.
Reporting and Documentation
- Prepares study reports and documentation.
- Maintains accurate records of study activities.
- Assists in the preparation of manuscripts and publications.
MARGINAL OR PERIODIC FUNCTIONS:
- Conducts literature reviews to support study design and protocol development.
- Assists in the training of new site staff and research team members.
- Participates in internal and external audits.
- Supports the development of study protocols and case report forms.
- Attends conferences and workshops to stay updated on industry trends.
- Adheres to internal controls and reporting structure.
- Performs related duties as required.
KNOWLEDGE/SKILLS/ABILITIES
- Double-checks work for errors, maintains organized records, and follows detailed procedures.
- Writes clear and concise reports, actively listens to others, and presents information effectively.
- Analyzes information, develops solutions, and implements corrective actions.
- Shares information, supports team decisions, and contributes to team success.
- Prioritizes tasks, sets realistic deadlines, and uses time efficiently.
REQUIRED QUALIFICATIONS
Requires a Bachelor's Degree in psychology, social work, public health, or a related field with at least 1 year(s) of experience in clinical research.
Relevant education and experience may be substituted as appropriate.
PREFERRED QUALIFICATIONS
- Master's Degree in psychology, social work, public health, or a related field with at least 2 year(s) of clinical research experience.
- Experience working with children, adolescents and young people who have a mental health condition.
- Fluent in Spanish.
- Certified Clinical Research Associate (CCRA) or Certified Clinical Research Professional (CCRP).
SALARY RANGE
$40,000 + depending on qualifications
WORKING CONDITIONS
- Standard office equipment
- Repetitive use of a keyboard
- Use of manual dexterity.
- Occasional weekends, overtime and evening work to meet deadlines
REQUIRED MATERIALS
- Resume/CV
- 3 work references with their contact information; at least one reference should be from a supervisor
- Letter of interest
Important for applicants who are NOT current university employees or contingent workers: You will be prompted to submit your resume the first time you apply, then you will be provided an option to upload a new Resume for subsequent applications. Any additional Required Materials (letter of interest, references, etc.) will be uploaded in the Application Questions section; you will be able to multi-select additional files. Before submitting your online job application, ensure that ALL Required Materials have been uploaded. Once your job application has been submitted, you cannot make changes.
Important for Current university employees and contingent workers: As a current university employee or contingent worker, you MUST apply within Workday by searching for Find UT Jobs. If you are a current University employee, log-in to Workday, navigate to your Worker Profile, click the Career link in the left hand navigation menu and then update the sections in your Professional Profile before you apply. This information will be pulled in to your application. The application is one page and you will be prompted to upload your resume. In addition, you must respond to the application questions presented to upload any additional Required Materials (letter of interest, references, etc.) that were noted above.
EMPLOYMENT ELIGIBILITY:
Regular staff who have been employed in their current position for the last six continuous months are eligible for openings being recruited for through University-Wide or Open Recruiting, to include both promotional opportunities and lateral transfers. Staff who are promotion/transfer eligible may apply for positions without supervisor approval.
RETIREMENT PLAN ELIGIBILITY:
The retirement plan for this position is Teacher Retirement System of Texas (TRS), subject to the position being at least 20 hours per week and at least 135 days in length.
BACKGROUND CHECKS:
A criminal history background check will be required for finalist(s) under consideration for this position.
EQUAL OPPORTUNITY EMPLOYER:
The University of Texas at Austin, as an equal opportunity/affirmative action employer, complies with all applicable federal and state laws regarding nondiscrimination and affirmative action. The University is committed to a policy of equal opportunity for all persons and does not discriminate on the basis of race, color, national origin, age, marital status, sex, sexual orientation, gender identity, gender expression, disability, religion, or veteran status in employment, educational programs and activities, and admissions.
PAY TRANSPARENCY:
The University of Texas at Austin will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information.
EMPLOYMENT ELIGIBILITY VERIFICATION:
If hired, you will be required to complete the federal Employment Eligibility Verification I-9 form. You will be required to present acceptable and original documents to prove your identity and authorization to work in the United States. Documents need to be presented no later than the third day of employment. Failure to do so will result in loss of employment at the university.
E-VERIFY:
The University of Texas at Austin uses E-Verify to check the work authorization of all new hires effective May 2015. The university’s company ID number for purposes of E-Verify is 854197. For more information about E-Verify, please see the following:
- E-Verify Poster (English and Spanish) [PDF]
- Right to Work Poster (English) [PDF]
- Right to Work Poster (Spanish) [PDF]
COMPLIANCE:
Employees may be required to report violations of law under Title IX and the Jeanne Clery Disclosure of Campus Security Policy and Crime Statistics Act (Clery Act). If this position is identified as a Campus Security Authority (Clery Act), you will be notified and provided resources for reporting. Responsible employees under Title IX are defined and outlined in HOP-3031.
The Clery Act requires all prospective employees to be notified of the availability of the Annual Security and Fire Safety report. You may access the most recent report here or obtain a copy at University Compliance Services, 1616 Guadalupe Street, UTA 2.206, Austin, Texas 78701.
Clinical Research Associate Job Roles in Texas
See all 138+ Clinical Research Associate Jobs 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 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.
See which clinical research associate employers are hiring and sponsoring visas in Texas right now.
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