Research Jobs at University of Texas Medical Branch with Visa Sponsorship
University of Texas Medical Branch runs an active research enterprise spanning clinical trials, biomedical science, and public health, giving Research professionals access to serious scientific infrastructure. UTMB has a consistent track record of sponsoring international researchers across multiple visa categories, making it a realistic target for candidates who need work authorization.
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Minimum Qualifications:
Master’s or doctoral degree in a related field, 7 years of related experience, and 4 years of progressive management and research experience.
Job Description:
The Assistant Director of Departmental Research is responsible for the operational oversight of clinical, translational, and basic science research within the Department. Current sites include all UTMB locations including Galveston, Clear Lake, League City and Angleton. The Assistant Director provides overall strategic and operational leadership to support the clinical, translational, and basic science research endeavors of the Department.
Job Duties:
- Establish standards of research conduct and practice for all research sites within their department.
- Establish mechanisms to ensure research is conducted in accordance with Institutional policies and procedures and applicable federal and local agencies, laws, and regulations for the protection of human subjects including the Office for Human Research Protections (OHRP), Food and Drug Administration (FDA), National Institutes of Health (NIH), UTMB Institutional Review Board (IRB), and the UTMB Human Research Protection Program.
- Integrate a system of operating and monitoring controls related to clinical research including proposal development, review, and post-award billing controls.
- Take a leadership role in ensuring clinical research programs and related support areas have high quality and integrity in compliance with Federal, State, and University guidelines.
- Stay abreast of new guidelines and best practices in the management of conflict of interests and in the protection of human subjects as they relate to the operational aspects of clinical research in the Department.
- Accountable for strategic planning, budgeting, quality assurance, and administration of activities and personnel that affect research protocols and patients, and the development of the assigned staff.
- Manage research facilities (clinical research lab, clinic space, research storage) and equipment including maintenance schedules.
- Coordinate emergency preparedness plans.
- Work with physician leaders and Principal Investigators to ensure all human subjects research activities are appropriate; and, to evaluate regulatory and compliance requirements of research protocols and clinical research care systems.
- Manage the clinical and translational research activities at all UTMB campuses and clinic sites for the department.
- Develop and maintain harmonious professional and productive relationships Institution-wide; build contacts important to achieving work goals; demonstrate diplomacy and tact.
- Serve as the effective formal and informal leader of teams and groups; obtain commitment and cooperation; delegate effectively; interview, hire, counsel, and evaluate personnel within assigned areas.
- Build and implement efficient workflows and system processes to meet research aims and effectively produce research outcomes.
- Actively promote collaboration between clinicians, research scientists, and other stakeholders internal and external to the University.
- Maintain relationships and coordinate collaboration among leaders of multidisciplinary teams including nursing, medical, pharmacy, clinical lab, scientific lab, business administration, and regulatory affairs.
- Prepare for and oversee federal and local regulatory agency (FDA, NIH, etc.) audits and inspections, compose responses, and prepare action plans to address findings.
- Participate in Departmental and Institutional committees with direct impact on research at UTMB, including the Departmental Research Committee which reviews funding opportunities and proposals, and advises on the research direction and priorities of the Department.
- Evaluate and support the development of grant opportunities; review and compose documents for grant applications and progress reports.
- Complete feasibility assessments and develop study budgets for NIH and industry-funded projects.
- Manage research education and development, including training, and mentorship for faculty, staff, fellows, and residents.
- Foster research development for the Department’s Fellowships and Residency Program; may assist in idea generation and trial start-up.
- Coordinate and supervise the development of research protocols, including study design, development of research questions, regulatory and Institutional Review Board (IRB) requirements, evaluation of resource requirements, and budgeting.
- May direct the conduct of research protocols and provide direction and supervision to the research team on initiating research study and protocol-related activities.
- Coordinates the schedules of research nurses and staff to ensure adequate coverage of protocols.
- Assists with ongoing strategic initiatives, including the Institutional Research Strategic Plan; ensures maintenance and stabilization of current infrastructure and planning for future growth and changes utilizing performance metrics and process improvement techniques.
- Manage Human Resources activities or give input for direct reports related to recruiting and selection, hiring and termination, training, professional development, mentoring, counseling, performance evaluations, and salary planning.
- Serves on NIH study sub-committees; actively participates in protocol and operations development, ensuring study procedures are feasible for participants, takes part in central outcome review, and manuscript review.
- Attends and participates in the Investigator planning meetings, pre-site, and site initiation visits.
- Reports adverse events appropriately and timely.
- Reviews goals and requirements of any new protocol, plans and designs source documentation for protocol, and adheres to protocols.
- Supervises preparation of all IRB and Regulatory Documents; under the direction of PI may draft various communications with Sponsor, and participates in the revision, development, and implementation of documents tools.
- Maintains regulatory certification and training for conduct of human subject research.
Marginal or Periodic Functions:
- Adheres to internal controls and reporting structure.
- Performs related duties as required.
KNOWLEDGE/SKILLS/ABILITIES:
- Excellent communication, interpersonal, and problem-solving skills with a high degree of professionalism and competence in dealing with faculty and employees at all levels.
- Proven ability to foster collaborative and constructive relationships.
- Proficiency in balancing complex federal, state, and local regulations, and industry sponsor requirements with Institutional policies and procedures to support and facilitate a world-class clinical research environment.
- Knowledge of and ability to function in a collaborative/participatory management environment in order to identify and resolve problems and develop plans, objectives, strategies, tactics, forecasts, and budgets.
- Ability to leverage personal skills to achieve high-level results, specifically personal skills in management planning, understanding of academic medical research environment, requirements, and challenges, and ability to overcome barriers to timely and productive results.
- Ability to prepare and analyze operating budgets, analyze/evaluate operational data, and utilize this information to make appropriate decisions and recommendations.
- Exceptional organizational skills with a focus on results that ensure timely progress on priorities. Ability to get things done and a track record of having done so.
- Embraces a compliance culture focused on education, facilitation, and customer service.
- Exceptional professional and personal ethics.
- Breadth and in-depth knowledge of clinical research quality systems, programs, and trends in an academic environment.
Preferred Qualifications:
- Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Professional (CCRP), or similar.
Salary Range:
Commensurate with experience.
EQUAL EMPLOYMENT OPPORTUNITY:
UTMB Health strives to provide equal opportunity employment without regard to race, color, religion, age, national origin, sex, gender, sexual orientation, gender identity/expression, genetic information, disability, veteran status, or any other basis protected by institutional policy or by federal, state or local laws unless such distinction is required by law. As a Federal Contractor, UTMB Health takes affirmative action to hire and advance protected veterans and individuals with disabilities.

Minimum Qualifications:
Master’s or doctoral degree in a related field, 7 years of related experience, and 4 years of progressive management and research experience.
Job Description:
The Assistant Director of Departmental Research is responsible for the operational oversight of clinical, translational, and basic science research within the Department. Current sites include all UTMB locations including Galveston, Clear Lake, League City and Angleton. The Assistant Director provides overall strategic and operational leadership to support the clinical, translational, and basic science research endeavors of the Department.
Job Duties:
- Establish standards of research conduct and practice for all research sites within their department.
- Establish mechanisms to ensure research is conducted in accordance with Institutional policies and procedures and applicable federal and local agencies, laws, and regulations for the protection of human subjects including the Office for Human Research Protections (OHRP), Food and Drug Administration (FDA), National Institutes of Health (NIH), UTMB Institutional Review Board (IRB), and the UTMB Human Research Protection Program.
- Integrate a system of operating and monitoring controls related to clinical research including proposal development, review, and post-award billing controls.
- Take a leadership role in ensuring clinical research programs and related support areas have high quality and integrity in compliance with Federal, State, and University guidelines.
- Stay abreast of new guidelines and best practices in the management of conflict of interests and in the protection of human subjects as they relate to the operational aspects of clinical research in the Department.
- Accountable for strategic planning, budgeting, quality assurance, and administration of activities and personnel that affect research protocols and patients, and the development of the assigned staff.
- Manage research facilities (clinical research lab, clinic space, research storage) and equipment including maintenance schedules.
- Coordinate emergency preparedness plans.
- Work with physician leaders and Principal Investigators to ensure all human subjects research activities are appropriate; and, to evaluate regulatory and compliance requirements of research protocols and clinical research care systems.
- Manage the clinical and translational research activities at all UTMB campuses and clinic sites for the department.
- Develop and maintain harmonious professional and productive relationships Institution-wide; build contacts important to achieving work goals; demonstrate diplomacy and tact.
- Serve as the effective formal and informal leader of teams and groups; obtain commitment and cooperation; delegate effectively; interview, hire, counsel, and evaluate personnel within assigned areas.
- Build and implement efficient workflows and system processes to meet research aims and effectively produce research outcomes.
- Actively promote collaboration between clinicians, research scientists, and other stakeholders internal and external to the University.
- Maintain relationships and coordinate collaboration among leaders of multidisciplinary teams including nursing, medical, pharmacy, clinical lab, scientific lab, business administration, and regulatory affairs.
- Prepare for and oversee federal and local regulatory agency (FDA, NIH, etc.) audits and inspections, compose responses, and prepare action plans to address findings.
- Participate in Departmental and Institutional committees with direct impact on research at UTMB, including the Departmental Research Committee which reviews funding opportunities and proposals, and advises on the research direction and priorities of the Department.
- Evaluate and support the development of grant opportunities; review and compose documents for grant applications and progress reports.
- Complete feasibility assessments and develop study budgets for NIH and industry-funded projects.
- Manage research education and development, including training, and mentorship for faculty, staff, fellows, and residents.
- Foster research development for the Department’s Fellowships and Residency Program; may assist in idea generation and trial start-up.
- Coordinate and supervise the development of research protocols, including study design, development of research questions, regulatory and Institutional Review Board (IRB) requirements, evaluation of resource requirements, and budgeting.
- May direct the conduct of research protocols and provide direction and supervision to the research team on initiating research study and protocol-related activities.
- Coordinates the schedules of research nurses and staff to ensure adequate coverage of protocols.
- Assists with ongoing strategic initiatives, including the Institutional Research Strategic Plan; ensures maintenance and stabilization of current infrastructure and planning for future growth and changes utilizing performance metrics and process improvement techniques.
- Manage Human Resources activities or give input for direct reports related to recruiting and selection, hiring and termination, training, professional development, mentoring, counseling, performance evaluations, and salary planning.
- Serves on NIH study sub-committees; actively participates in protocol and operations development, ensuring study procedures are feasible for participants, takes part in central outcome review, and manuscript review.
- Attends and participates in the Investigator planning meetings, pre-site, and site initiation visits.
- Reports adverse events appropriately and timely.
- Reviews goals and requirements of any new protocol, plans and designs source documentation for protocol, and adheres to protocols.
- Supervises preparation of all IRB and Regulatory Documents; under the direction of PI may draft various communications with Sponsor, and participates in the revision, development, and implementation of documents tools.
- Maintains regulatory certification and training for conduct of human subject research.
Marginal or Periodic Functions:
- Adheres to internal controls and reporting structure.
- Performs related duties as required.
KNOWLEDGE/SKILLS/ABILITIES:
- Excellent communication, interpersonal, and problem-solving skills with a high degree of professionalism and competence in dealing with faculty and employees at all levels.
- Proven ability to foster collaborative and constructive relationships.
- Proficiency in balancing complex federal, state, and local regulations, and industry sponsor requirements with Institutional policies and procedures to support and facilitate a world-class clinical research environment.
- Knowledge of and ability to function in a collaborative/participatory management environment in order to identify and resolve problems and develop plans, objectives, strategies, tactics, forecasts, and budgets.
- Ability to leverage personal skills to achieve high-level results, specifically personal skills in management planning, understanding of academic medical research environment, requirements, and challenges, and ability to overcome barriers to timely and productive results.
- Ability to prepare and analyze operating budgets, analyze/evaluate operational data, and utilize this information to make appropriate decisions and recommendations.
- Exceptional organizational skills with a focus on results that ensure timely progress on priorities. Ability to get things done and a track record of having done so.
- Embraces a compliance culture focused on education, facilitation, and customer service.
- Exceptional professional and personal ethics.
- Breadth and in-depth knowledge of clinical research quality systems, programs, and trends in an academic environment.
Preferred Qualifications:
- Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Professional (CCRP), or similar.
Salary Range:
Commensurate with experience.
EQUAL EMPLOYMENT OPPORTUNITY:
UTMB Health strives to provide equal opportunity employment without regard to race, color, religion, age, national origin, sex, gender, sexual orientation, gender identity/expression, genetic information, disability, veteran status, or any other basis protected by institutional policy or by federal, state or local laws unless such distinction is required by law. As a Federal Contractor, UTMB Health takes affirmative action to hire and advance protected veterans and individuals with disabilities.
See all 27+ Research at University of Texas Medical Branch jobs
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Get Access To All JobsTips for Finding Research Jobs at University of Texas Medical Branch Jobs
Align your credentials to UTMB's research priorities
UTMB's research spans infectious disease, aging, cancer, and public health. Before applying, map your academic background and publications directly to active labs or departments. Hiring managers in research settings weigh scientific fit as heavily as immigration eligibility.
Verify your degree qualifies as a specialty occupation
H-1B approval for Research roles requires USCIS to confirm your position qualifies as a specialty occupation. A doctorate or highly specialized master's degree in a directly related field strengthens your petition considerably compared to a general science background.
Target postdoctoral and staff scientist postings specifically
UTMB's Research hiring frequently flows through postdoctoral fellowship and staff scientist tracks, which are the entry points most likely to come with built-in sponsorship pathways. Filter your search to these designations rather than applying broadly across all research-adjacent titles.
Use Migrate Mate to find open Research roles at UTMB
Rather than monitoring UTMB's careers portal manually, use Migrate Mate to surface Research openings at UTMB filtered by visa sponsorship type, so you can prioritize applications to roles already aligned with your authorization needs.
Clarify sponsorship scope before accepting an offer
Ask your hiring contact whether the offer covers only H-1B filing or also includes premium processing and future Green Card sponsorship. Research positions at academic medical centers sometimes limit PERM-based sponsorship to tenured or permanent staff classifications.
Account for LCA certification time in your start date negotiation
Your employer must file a certified Labor Condition Application with DOL before USCIS can adjudicate your H-1B petition. This step alone can take one to three weeks, so build that buffer into any start date you negotiate during the offer stage.
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Find Research at University of Texas Medical Branch JobsFrequently Asked Questions
Does University of Texas Medical Branch sponsor H-1B visas for Researchs?
Yes, University of Texas Medical Branch sponsors H-1B visas for qualifying Research positions. As a large academic medical institution, UTMB has established immigration processes and works with legal counsel to support petitions for researchers in specialty occupation roles. Your position must require a bachelor's degree or higher in a specific field directly related to the job duties.
How do I apply for Research jobs at University of Texas Medical Branch?
You can find and apply for Research roles at University of Texas Medical Branch through UTMB's official careers portal or through Migrate Mate, which filters open positions by visa sponsorship type so you can identify roles where H-1B or OPT support is already expected. Tailor your application to the specific lab, department, or research focus area listed in the posting.
Which visa types does University of Texas Medical Branch commonly use for Research roles?
UTMB sponsors H-1B visas for Research professionals in specialty occupation roles, and also supports F-1 OPT and F-1 CPT for students and recent graduates completing research-related degrees. TN status is available for Canadian and Mexican nationals in qualifying research classifications. The right category depends on your nationality, degree level, and the specific position offered.
What qualifications does UTMB expect for Research positions?
Research roles at UTMB typically require a graduate degree, often a master's or doctorate, in a field directly relevant to the position. For laboratory and clinical research roles, hands-on experience with specific methodologies, prior publications, or postdoctoral training can be decisive. Generalist science backgrounds without a direct field match are less likely to clear USCIS specialty occupation review.
How do I time my application if my OPT or H-1B status is expiring?
If you're on F-1 OPT, the 60-day grace period after employment ends gives you limited time to secure a new role and begin a new authorization period. For H-1B, portability rules allow you to change employers once a new petition is filed. At a large institution like UTMB, internal HR processing can add weeks before an immigration petition is submitted, so engage early and ask about their typical filing timeline.
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