Clinical Support Associate Visa Sponsorship Jobs in Connecticut
Connecticut's clinical support associate jobs are concentrated around major health systems like Yale New Haven Health, Hartford HealthCare, and Nuvance Health. Employers in New Haven, Hartford, and Bridgeport regularly hire for these roles, and some sponsor work visas for qualified international candidates with clinical backgrounds and relevant credentials.
See All Clinical Support Associate JobsOverview
Showing 5 of 54+ Clinical Support Associate Jobs in Connecticut with Visa Sponsorship jobs


Have you applied for this role?


Have you applied for this role?


Have you applied for this role?


Have you applied for this role?


Have you applied for this role?
See all 54+ Clinical Support Associate Jobs in Connecticut with Visa Sponsorship
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Clinical Support Associate Jobs in Connecticut with Visa Sponsorship.
Get Access To All Jobs
INTRODUCTION
Working at Yale means contributing to a better tomorrow. Whether you are a current resident of our New Haven-based community, eligible for opportunities through the New Haven Hiring Initiative, or a newcomer, interested in exploring all that Yale has to offer, your talents and contributions are welcome. Discover your opportunities at Yale!
Overview
The anticipated salary range for this position is up to $75,000, depending on experience and qualifications. Yale offers a comprehensive benefits package.
The Clinical Research Support Laboratory (CRSL) is the primary non-CLIA certified laboratory responsible for collecting, processing, stabilizing, documenting, shipping and tracking all research biospecimens from patients participating in therapeutic clinical trials supported by the Yale Cancer Center Clinical Trials Office.
Reporting to the CRSL Laboratory Supervisor, the Research Associate is responsible for managing the central research specimen requirements for the CTO’s portfolio of studies. With a high degree of independence, the Research Associate will serve as primary interface between the clinical operations and laboratory settings to provide meticulous preparation, coordination, and shipment of biological specimens obtained from patients participating in clinical oncology trials. This position requires comprehending and following protocols and laboratory manuals for a large number of clinical studies with a high degree of accuracy. Responsibilities include collaboration with CRSL Management for creating tools and facilitating logistical and workflow considerations for the laboratory to determine the necessary resources required to implement and maintain the study at the Smilow Cancer Hospital in New Haven as well as across the network sites. The Research Associate will provide oversight of daily operations across assigned Clinical Research Support Laboratory locations, including network and New Haven sites. The Research Associate will assist with processing and shipping biological specimens at New Haven and network sites as assigned. Travel to different laboratory locations will be required. Supervisory responsibilities of one or more staff assigned to work at designated locations may be required.
Essential Duties
- Recommends the design and implementation of procedures and protocols under the direction of a higher-level authority.
- Investigates, analyzes, and reaches preliminary scientific conclusions related to research planning.
- Ensures data results are compiled, analyzed, and presented properly.
- Analyzes, develops and interprets scientific results. Maintains clear documentation of results. Prepares scientific reports and papers for research proposals and published reports.
- Performs independent research and laboratory techniques and participates in experimental research planning.
- Interacts with internal contacts including the PI, research assistants, graduate students, Radiation Safety and Biological Safety officers, and Animal Care personnel to discuss and evaluate research results and to ensure the smooth and safe operation of the laboratory.
- Interacts with external contacts such as researchers at other institutions, staff at biotechnology and reagents companies to consult on research methods and to keep abreast of product information and developments.
- Interacts with University personnel to define work assignments and requirements, communicate progress of work, and plan and coordinate projects.
- Maintains equipment and supplies for unit.
- May perform other duties as assigned.
Required Skills and Abilities
- Excellent interpersonal skills and ability to relay information to/obtain information from internal Yale staff as well as external study staff, including physicians, research staff, and study sponsors.
- Strong analytic and critical thinking skills. Proven ability to comprehend complex clinical trial laboratory manuals and associated materials and protocols with a demonstrated ability to extract relevant information.
- Demonstrated knowledge of medical and laboratory terminology. Proven ability to work in a laboratory, preferably in a BSL-2 laboratory. Ability to travel to different laboratory locations to supervise, manage, and oversee work of one or more staff; a valid driver’s license and the ability to use of one's own motor vehicle is required.
- Excellent time management and organizational skills. Ability to meet daily deadlines while handling multiple projects. Proven ability to manage several projects concurrently, while balancing competing priorities and deadlines. Extreme flexibility in work focus; ability to switch among several different projects without any adverse effects.
PREFERRED EDUCATION, EXPERIENCE AND SKILLS:
- Bachelor's Degree in a related field and three years or more experience.
- Previous supervisory experience, particularly in a laboratory setting.
- Previous clinical trials experience and/or experience in an oncology setting.
- Previous experience with supply management and shipping regulations.
Principal Responsibilities
- Recommends the design and implementation of procedures and protocols under the direction of a higher-level authority.
- Investigates, analyzes, and reaches preliminary scientific conclusions related to research planning.
- Ensures data results are compiled, analyzed, and presented properly.
- Analyzes, develops and interprets scientific results. Maintains clear documentation of results. Prepares scientific reports and papers for research proposals and published reports.
- Performs independent research and laboratory techniques and participates in experimental research planning.
- Interacts with internal contacts including the PI, research assistants, graduate students, Radiation Safety and Biological Safety officers, and Animal Care personnel to discuss and evaluate research results and to ensure the smooth and safe operation of the laboratory.
- Interacts with external contacts such as researchers at other institutions, staff at biotechnology and reagents companies to consult on research methods and to keep abreast of product information and developments.
- May perform other duties as assigned.
Required Education and Experience
Master’s Degree in a scientific discipline and one year experience or an equivalent combination of education and experience.
Job Posting Date
03/30/2026
Job Category
Professional
Bargaining Unit
NON
Compensation Grade
Clinical & Research
Compensation Grade Profile
Research Associate 1 MS (22)
Salary Range
$61,500.00 - $91,875.00
Time Type
Full time
Duration Type
Staff
Work Model
On-site
Background Check Requirements
All candidates for employment will be subject to pre-employment background screening for this position, which may include motor vehicle, DOT certification, drug testing and credit checks based on the position description and job requirements. All offers are contingent upon the successful completion of the background check. For additional information on the background check requirements and process visit "Learn about background checks" under the Applicant Support Resources section of Careers on the It's Your Yale website.
Health Requirements
This role is a healthcare worker position. Healthcare workers (HCW) are defined as university employees working a healthcare setting who have the potential for direct or indirect exposure to patients, human research subjects or infectious materials including body substance, contaminated medical supplies, devices and equipment, surfaces, or air. HCW have specific health requirements that must be met prior to starting work, including MMR vaccine or immunity, varicella (chickenpox) vaccine or immunity, TB screening, COVID vaccine according to University policy, hepatitis B vaccine or immunity, and annual flu vaccination.
Posting Disclaimer
Salary offers are determined by a candidate’s qualifications, experience, skills, and education in relation to the position requirements, along with the role’s grade profile and current internal and external market conditions.
The intent of this job description is to provide a representative summary of the essential functions that will be required of the position and should not be construed as a declaration of specific duties and responsibilities of the position. Employees will be assigned specific job-related duties through their hiring department.
The University is committed to basing judgments concerning the admission, education, and employment of individuals upon their qualifications and abilities and seeks to attract to its faculty, staff, and student body qualified persons from a broad range of backgrounds and perspectives. In accordance with this policy and as delineated by federal and Connecticut law, Yale does not discriminate in admissions, educational programs, or employment against any individual on account of that individual’s sex, sexual orientation, gender identity or expression, race, color, national or ethnic origin, religion, age, disability, status as a special disabled veteran, veteran of the Vietnam era or other covered veteran.
Inquiries concerning Yale's Policy Against Discrimination and Harassment may be referred to the Office of Institutional Equity and Accessibility (OIEA).
Yale University is a tobacco-free campus.

INTRODUCTION
Working at Yale means contributing to a better tomorrow. Whether you are a current resident of our New Haven-based community, eligible for opportunities through the New Haven Hiring Initiative, or a newcomer, interested in exploring all that Yale has to offer, your talents and contributions are welcome. Discover your opportunities at Yale!
Overview
The anticipated salary range for this position is up to $75,000, depending on experience and qualifications. Yale offers a comprehensive benefits package.
The Clinical Research Support Laboratory (CRSL) is the primary non-CLIA certified laboratory responsible for collecting, processing, stabilizing, documenting, shipping and tracking all research biospecimens from patients participating in therapeutic clinical trials supported by the Yale Cancer Center Clinical Trials Office.
Reporting to the CRSL Laboratory Supervisor, the Research Associate is responsible for managing the central research specimen requirements for the CTO’s portfolio of studies. With a high degree of independence, the Research Associate will serve as primary interface between the clinical operations and laboratory settings to provide meticulous preparation, coordination, and shipment of biological specimens obtained from patients participating in clinical oncology trials. This position requires comprehending and following protocols and laboratory manuals for a large number of clinical studies with a high degree of accuracy. Responsibilities include collaboration with CRSL Management for creating tools and facilitating logistical and workflow considerations for the laboratory to determine the necessary resources required to implement and maintain the study at the Smilow Cancer Hospital in New Haven as well as across the network sites. The Research Associate will provide oversight of daily operations across assigned Clinical Research Support Laboratory locations, including network and New Haven sites. The Research Associate will assist with processing and shipping biological specimens at New Haven and network sites as assigned. Travel to different laboratory locations will be required. Supervisory responsibilities of one or more staff assigned to work at designated locations may be required.
Essential Duties
- Recommends the design and implementation of procedures and protocols under the direction of a higher-level authority.
- Investigates, analyzes, and reaches preliminary scientific conclusions related to research planning.
- Ensures data results are compiled, analyzed, and presented properly.
- Analyzes, develops and interprets scientific results. Maintains clear documentation of results. Prepares scientific reports and papers for research proposals and published reports.
- Performs independent research and laboratory techniques and participates in experimental research planning.
- Interacts with internal contacts including the PI, research assistants, graduate students, Radiation Safety and Biological Safety officers, and Animal Care personnel to discuss and evaluate research results and to ensure the smooth and safe operation of the laboratory.
- Interacts with external contacts such as researchers at other institutions, staff at biotechnology and reagents companies to consult on research methods and to keep abreast of product information and developments.
- Interacts with University personnel to define work assignments and requirements, communicate progress of work, and plan and coordinate projects.
- Maintains equipment and supplies for unit.
- May perform other duties as assigned.
Required Skills and Abilities
- Excellent interpersonal skills and ability to relay information to/obtain information from internal Yale staff as well as external study staff, including physicians, research staff, and study sponsors.
- Strong analytic and critical thinking skills. Proven ability to comprehend complex clinical trial laboratory manuals and associated materials and protocols with a demonstrated ability to extract relevant information.
- Demonstrated knowledge of medical and laboratory terminology. Proven ability to work in a laboratory, preferably in a BSL-2 laboratory. Ability to travel to different laboratory locations to supervise, manage, and oversee work of one or more staff; a valid driver’s license and the ability to use of one's own motor vehicle is required.
- Excellent time management and organizational skills. Ability to meet daily deadlines while handling multiple projects. Proven ability to manage several projects concurrently, while balancing competing priorities and deadlines. Extreme flexibility in work focus; ability to switch among several different projects without any adverse effects.
PREFERRED EDUCATION, EXPERIENCE AND SKILLS:
- Bachelor's Degree in a related field and three years or more experience.
- Previous supervisory experience, particularly in a laboratory setting.
- Previous clinical trials experience and/or experience in an oncology setting.
- Previous experience with supply management and shipping regulations.
Principal Responsibilities
- Recommends the design and implementation of procedures and protocols under the direction of a higher-level authority.
- Investigates, analyzes, and reaches preliminary scientific conclusions related to research planning.
- Ensures data results are compiled, analyzed, and presented properly.
- Analyzes, develops and interprets scientific results. Maintains clear documentation of results. Prepares scientific reports and papers for research proposals and published reports.
- Performs independent research and laboratory techniques and participates in experimental research planning.
- Interacts with internal contacts including the PI, research assistants, graduate students, Radiation Safety and Biological Safety officers, and Animal Care personnel to discuss and evaluate research results and to ensure the smooth and safe operation of the laboratory.
- Interacts with external contacts such as researchers at other institutions, staff at biotechnology and reagents companies to consult on research methods and to keep abreast of product information and developments.
- May perform other duties as assigned.
Required Education and Experience
Master’s Degree in a scientific discipline and one year experience or an equivalent combination of education and experience.
Job Posting Date
03/30/2026
Job Category
Professional
Bargaining Unit
NON
Compensation Grade
Clinical & Research
Compensation Grade Profile
Research Associate 1 MS (22)
Salary Range
$61,500.00 - $91,875.00
Time Type
Full time
Duration Type
Staff
Work Model
On-site
Background Check Requirements
All candidates for employment will be subject to pre-employment background screening for this position, which may include motor vehicle, DOT certification, drug testing and credit checks based on the position description and job requirements. All offers are contingent upon the successful completion of the background check. For additional information on the background check requirements and process visit "Learn about background checks" under the Applicant Support Resources section of Careers on the It's Your Yale website.
Health Requirements
This role is a healthcare worker position. Healthcare workers (HCW) are defined as university employees working a healthcare setting who have the potential for direct or indirect exposure to patients, human research subjects or infectious materials including body substance, contaminated medical supplies, devices and equipment, surfaces, or air. HCW have specific health requirements that must be met prior to starting work, including MMR vaccine or immunity, varicella (chickenpox) vaccine or immunity, TB screening, COVID vaccine according to University policy, hepatitis B vaccine or immunity, and annual flu vaccination.
Posting Disclaimer
Salary offers are determined by a candidate’s qualifications, experience, skills, and education in relation to the position requirements, along with the role’s grade profile and current internal and external market conditions.
The intent of this job description is to provide a representative summary of the essential functions that will be required of the position and should not be construed as a declaration of specific duties and responsibilities of the position. Employees will be assigned specific job-related duties through their hiring department.
The University is committed to basing judgments concerning the admission, education, and employment of individuals upon their qualifications and abilities and seeks to attract to its faculty, staff, and student body qualified persons from a broad range of backgrounds and perspectives. In accordance with this policy and as delineated by federal and Connecticut law, Yale does not discriminate in admissions, educational programs, or employment against any individual on account of that individual’s sex, sexual orientation, gender identity or expression, race, color, national or ethnic origin, religion, age, disability, status as a special disabled veteran, veteran of the Vietnam era or other covered veteran.
Inquiries concerning Yale's Policy Against Discrimination and Harassment may be referred to the Office of Institutional Equity and Accessibility (OIEA).
Yale University is a tobacco-free campus.
Clinical Support Associate Job Roles in Connecticut
See all 54+ Clinical Support Associate Jobs in Connecticut
Sign up for free to filter by visa type, set job alerts, and find employers with verified sponsorship history.
Search Clinical Support Associate Jobs in ConnecticutClinical Support Associate Jobs in Connecticut: Frequently Asked Questions
Which companies sponsor visas for clinical support associates in Connecticut?
Yale New Haven Health, Hartford HealthCare, and Nuvance Health are among the larger health systems in Connecticut with documented H-1B sponsorship histories across clinical roles. Academic medical centers affiliated with Yale School of Medicine and UConn Health also sponsor international workers in clinical support positions, though sponsorship decisions vary by department, role classification, and candidate qualifications.
Which visa types are most common for clinical support associate roles in Connecticut?
The H-1B is the most common work visa for clinical support associates in Connecticut, provided the role qualifies as a specialty occupation requiring at least a bachelor's degree in a relevant field such as health sciences, biology, or a related discipline. TN visas apply to Canadian and Mexican nationals in eligible clinical occupations. Some candidates already on OPT or STEM OPT also work in these roles while seeking full sponsorship.
Which cities in Connecticut have the most clinical support associate sponsorship jobs?
New Haven has the highest concentration of clinical support associate opportunities due to Yale New Haven Hospital and the broader Yale medical campus. Hartford follows closely, anchored by Hartford HealthCare and Saint Francis Hospital. Bridgeport, Danbury, and Norwalk also have active hiring through Nuvance Health and smaller regional health systems, making Fairfield County a secondary hub worth targeting.
How to find clinical support associate visa sponsorship jobs in Connecticut?
Migrate Mate is designed specifically for international candidates searching for visa sponsorship jobs, including clinical support associate roles in Connecticut. You can filter by state and role to see positions where employers have indicated sponsorship willingness. Focusing your search on large academic medical centers and multi-site health systems in New Haven and Hartford increases your chances of finding roles with active sponsorship programs.
Are there any Connecticut-specific considerations for clinical support associates seeking visa sponsorship?
Connecticut's clinical job market is heavily tied to academic medicine, which means employers like Yale New Haven and UConn Health are accustomed to sponsoring international hires and navigating prevailing wage requirements. Roles in Connecticut's Fairfield County may face higher prevailing wage benchmarks given proximity to New York City. Candidates with degrees from Connecticut's universities, including UConn and Quinnipiac, may also benefit from established employer pipelines into clinical support roles.
What is the prevailing wage for sponsored clinical support associate jobs in Connecticut?
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 support associate employers are hiring and sponsoring visas in Connecticut right now.
Search Clinical Support Associate Jobs in Connecticut