Research Visa Sponsorship Jobs in Tennessee
Research visa sponsorship jobs in Tennessee are concentrated around Nashville, Memphis, and Knoxville, where institutions like Vanderbilt University, St. Jude Children's Research Hospital, and Oak Ridge National Laboratory regularly sponsor international talent. Life sciences, biomedical research, and energy sectors drive most sponsorship activity across the state.
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Get Access To All JobsJOB SUMMARY/ESSENTIAL JOB FUNCTIONS:
The Research Project Coordinator for the ENRICH Project manages the day-to-day aspects of the clinical trial work specified, including IRB-related administration, regulatory compliance, case report form collection, oversight of integrity, and transfer of collected data to the Research Data Coordinator relevant research team coordination, and research data management/administrative responsibilities as directed and supervised by the project Principal Investigator.
- Coordinates research studies and assists in the design of studies by reviewing proposals to determine research methods.
- Participates in the recruitment and selection of study participants to determine compliance with eligibility requirements.
- Assists in the development of procedures for the design of measurement instruments and scoring systems.
- Establishes and maintains contact with project team, study sponsors, participants and families, community agencies, and health care providers.
- Implements research protocol, monitors participant adherence to protocols, and takes action to correct problems such as deviation from protocol requirements.
- Oversees study patient identification, screening, recruitment, enrollment, consenting, and direct communication with patients/caregivers during and after radiation treatment to record interruption events, and to interview patients/caregivers face-to-face or by phone to collect information about major interruption events.
- Coordinates communication between the oncology clinic nursing and radiotherapy treatment staff, project patient navigation team, and project data science team to record study outcomes and alert providers to any patient experiencing unplanned treatment interruption events.
- Communicates and collaborates with the study team including internal and external parties, sponsors, principal investigators, and study participants.
- Writes or reviews human subject applications and consent forms in compliance with applicable regulations.
- Complies with Good Clinical Practice Guidelines and FDA Guidelines regarding clinical research.
- Maintains all applicable trainings and certifications including but not limited to HIPAA Training, IATA hazardous materials shipping training, and CITI certification.
- Performs other duties as assigned.
MINIMUM REQUIREMENTS:
Education: Bachelor’s Degree in Social Work, Psychology, or Public Health. (TRANSCRIPT REQUIRED)
Experience: Two (2) years of related experience; OR Master’s Degree in lieu of experience; OR a combination of education and experience to equal six (6) years. Prior clinical and research team leadership experience, patient navigation experience, and/or successful demonstration of administrative skills are desirable but not required.
KNOWLEDGE, SKILLS, AND ABILITIES:
- Ability to successfully complete certifications in CITI Human Subjects Protection, CITI Good Clinical Practice, IATA Hazardous Materials Shipping, and HIPAA training.
- Skilled in clinical trial operations, clinical research team coordination, research budgeting and regulatory management, clinical patient assessment/consenting/interaction, research data collection, and fundamental public presentation skills.
- Computer skills including Microsoft Office Suite, as well as basic mastery of graphical user interfaces and relational database software.
WORK SCHEDULE: This position may occasionally be required to work weekends and evenings.
Market Range: 10
Hiring Salary: $4,182.12 - $5,655.25/Monthly
THIS IS A GRANT-FUNDED POSITION FUNDED UNTIL DECEMBER 31, 2026
JOB SUMMARY/ESSENTIAL JOB FUNCTIONS:
The Research Project Coordinator for the ENRICH Project manages the day-to-day aspects of the clinical trial work specified, including IRB-related administration, regulatory compliance, case report form collection, oversight of integrity, and transfer of collected data to the Research Data Coordinator relevant research team coordination, and research data management/administrative responsibilities as directed and supervised by the project Principal Investigator.
- Coordinates research studies and assists in the design of studies by reviewing proposals to determine research methods.
- Participates in the recruitment and selection of study participants to determine compliance with eligibility requirements.
- Assists in the development of procedures for the design of measurement instruments and scoring systems.
- Establishes and maintains contact with project team, study sponsors, participants and families, community agencies, and health care providers.
- Implements research protocol, monitors participant adherence to protocols, and takes action to correct problems such as deviation from protocol requirements.
- Oversees study patient identification, screening, recruitment, enrollment, consenting, and direct communication with patients/caregivers during and after radiation treatment to record interruption events, and to interview patients/caregivers face-to-face or by phone to collect information about major interruption events.
- Coordinates communication between the oncology clinic nursing and radiotherapy treatment staff, project patient navigation team, and project data science team to record study outcomes and alert providers to any patient experiencing unplanned treatment interruption events.
- Communicates and collaborates with the study team including internal and external parties, sponsors, principal investigators, and study participants.
- Writes or reviews human subject applications and consent forms in compliance with applicable regulations.
- Complies with Good Clinical Practice Guidelines and FDA Guidelines regarding clinical research.
- Maintains all applicable trainings and certifications including but not limited to HIPAA Training, IATA hazardous materials shipping training, and CITI certification.
- Performs other duties as assigned.
MINIMUM REQUIREMENTS:
Education: Bachelor’s Degree in Social Work, Psychology, or Public Health. (TRANSCRIPT REQUIRED)
Experience: Two (2) years of related experience; OR Master’s Degree in lieu of experience; OR a combination of education and experience to equal six (6) years. Prior clinical and research team leadership experience, patient navigation experience, and/or successful demonstration of administrative skills are desirable but not required.
KNOWLEDGE, SKILLS, AND ABILITIES:
- Ability to successfully complete certifications in CITI Human Subjects Protection, CITI Good Clinical Practice, IATA Hazardous Materials Shipping, and HIPAA training.
- Skilled in clinical trial operations, clinical research team coordination, research budgeting and regulatory management, clinical patient assessment/consenting/interaction, research data collection, and fundamental public presentation skills.
- Computer skills including Microsoft Office Suite, as well as basic mastery of graphical user interfaces and relational database software.
WORK SCHEDULE: This position may occasionally be required to work weekends and evenings.
Market Range: 10
Hiring Salary: $4,182.12 - $5,655.25/Monthly
THIS IS A GRANT-FUNDED POSITION FUNDED UNTIL DECEMBER 31, 2026
Research Job Roles in Tennessee
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Search Research Jobs in TennesseeResearch Jobs in Tennessee: Frequently Asked Questions
Which companies sponsor visas for research roles in Tennessee?
St. Jude Children's Research Hospital in Memphis is one of Tennessee's most active sponsors for research positions, particularly in oncology and biomedical sciences. Oak Ridge National Laboratory sponsors researchers in energy, materials science, and computational fields. Vanderbilt University Medical Center and the University of Tennessee system also sponsor international researchers, primarily for postdoctoral and staff scientist roles tied to federal grant funding.
Which visa types are most common for research roles in Tennessee?
The H-1B is the most common work visa for research positions in Tennessee, covering roles that require a specialized degree. J-1 visas are widely used for postdoctoral researchers and research scholars at universities and national laboratories, sponsored through institutional exchange programs. O-1A visas appear for researchers with extraordinary ability, particularly those with strong publication records or competitive grant awards. Many federally funded research institutions also hold cap-exempt H-1B status.
Which cities in Tennessee have the most research sponsorship jobs?
Nashville leads due to its concentration of research universities, medical centers, and a growing life sciences sector anchored by Vanderbilt. Oak Ridge, near Knoxville, is a specialized hub for federally funded scientific research through the Department of Energy. Memphis hosts significant biomedical and clinical research activity centered on St. Jude and the University of Tennessee Health Science Center. Knoxville itself also supports research hiring through the University of Tennessee's main campus.
How to find research visa sponsorship jobs in Tennessee?
Migrate Mate filters job listings specifically for roles with visa sponsorship, making it straightforward to search for research positions in Tennessee without sorting through listings that exclude international candidates. You can filter by state and research-related job categories to surface openings at institutions like Oak Ridge National Laboratory, Vanderbilt, and St. Jude. Focusing on federally affiliated employers and research universities tends to yield the highest concentration of sponsorship-eligible postings.
Are there state-specific considerations for research sponsorship jobs in Tennessee?
Tennessee has a strong pipeline from its research universities into sponsored roles, which means postdoctoral positions often serve as entry points for H-1B sponsorship at the same institution after J-1 completion. Oak Ridge National Laboratory operates under federal contractor hiring rules, which can affect visa processing timelines and security clearance requirements. Tennessee does not have a state income tax on wages, which is relevant context for understanding total compensation when evaluating offers.
What is the prevailing wage for sponsored research jobs in Tennessee?
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.
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