Clinical Research Visa Sponsorship Jobs in Rhode Island
Rhode Island's clinical research sector is anchored by Brown University's medical programs, Lifespan Health System, and Care New England, with major activity concentrated in Providence. Biotech and hospital-based research roles in this compact state regularly attract international talent, and employers here have an established history of sponsoring H-1B and other work visas for qualified clinical research professionals.
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SUMMARY
Reporting to the Principal Investigator(s), and in accordance with established policies and procedures, the incumbent is responsible for the operation of research programs, including recruitment, implementation programs, processes and outcome evaluation of the program.
Brown University Health employees are expected to successfully role model the organization's values of Compassion, Accountability, Respect, and Excellence as these values guide our everyday actions with patients, customers and one another.
In addition to our values, all employees are expected to demonstrate the core Success Factors which tell us how we work together and how we get things done. The core Success Factors include:
- Instill Trust and Value Differences
- Patient and Community Focus and Collaborate
Responsibilities
Brown University Health employees are expected to embrace Brown University Health's mission of Delivering health with care and successfully role model Brown University Health's values of Compassion, Accountability, Respect, and Excellence as these guide our everyday actions with patients, customers and one another.
- Assists Principal Investigator(s) with development, design and data management specifics of new studies and forms; may assist with tabulating and reviewing data results for publication and reporting.
- Also assists in developing grant applications, developing and managing budgets, subcontracts, and expenditures.
- Provides for training and orientation to research and grant procedures.
- Coordinates work schedule, monitors adherence to procedures/protocols.
- Provides input into development of performance evaluation for non-clinical aspects of staff assigned to project.
- Recommends corrective action as appropriate.
- May organize and implement aspects of research protocols and assist in coordinating clinical research projects, which may include: record review, establishing and maintaining research records, and entering data into computerized database.
- Assists research investigators in budgeting and managing financial accounts effectively within the guidelines and policies established by the Hospital as well as sponsoring agencies.
- Resolves problems and monitors monthly expense reports for accuracy and conformance to budget.
- Addresses variances as required to meet the grant budget.
- May prepare special analyses as appropriate.
- Coordinates all required submissions related to protocol, physicians and procedures to the protocol office – regulatory affairs.
- Coordinates collaborative work with other investigators and/or sites.
- Also coordinates audits and on-site visits by the pharmaceutical companies and any other appropriate groups.
- Maintains quality assurance, safety, environmental and infection control in accordance with established hospital department policies and objectives.
- Coordinates and/or conducts annual training in these areas.
- May require outside travel to evaluate sites or for other grant-related reasons.
- Maintains and enhances professional expertise through educational opportunities and review of pertinent literature.
MINIMUM QUALIFICATIONS
BASIC KNOWLEDGE: Masters Degree in relevant discipline or occupation is preferred. May consider relevant education and/or work experience year for year for degree. Excellent computer skills and familiarity with statistics. May require valid driver’s license where grant requires travel outside of hospital.
Experience: Three or more years progressively more responsible relevant experience, depending on size and complexity of program(s) or organization. Experience should demonstrate leadership skills and ability to effectively prepare and monitor budgets.
WORK ENVIRONMENT AND PHYSICAL REQUIREMENTS: While most duties are performed in an office environment, incumbent is exposed to patient care environment. Any risk of exposure to contagious or noxious elements is minimized by adherence to safety procedures and protocols.
INDEPENDENT ACTION: Incumbent functions independently within a broad scope of department policies and practices; generally refers specific problems to supervisor only where clarification of department policies and procedures may be required.
SUPERVISORY RESPONSIBILITY: May provide direct supervision for up to 3 full-time equivalent personnel assigned to the program.
Pay Range
$64,480.00-$106,412.80
Location
The Miriam Hospital - 164 Summit Ave Providence, Rhode Island 02906
Work Type
M-F 8am - 4:30pm
Work Shift
Day
Daily Hours
8 hours
Driving Required
No
Brown University Health is committed to providing equal employment opportunities and maintaining a work environment free from all forms of unlawful discrimination and harassment.

SUMMARY
Reporting to the Principal Investigator(s), and in accordance with established policies and procedures, the incumbent is responsible for the operation of research programs, including recruitment, implementation programs, processes and outcome evaluation of the program.
Brown University Health employees are expected to successfully role model the organization's values of Compassion, Accountability, Respect, and Excellence as these values guide our everyday actions with patients, customers and one another.
In addition to our values, all employees are expected to demonstrate the core Success Factors which tell us how we work together and how we get things done. The core Success Factors include:
- Instill Trust and Value Differences
- Patient and Community Focus and Collaborate
Responsibilities
Brown University Health employees are expected to embrace Brown University Health's mission of Delivering health with care and successfully role model Brown University Health's values of Compassion, Accountability, Respect, and Excellence as these guide our everyday actions with patients, customers and one another.
- Assists Principal Investigator(s) with development, design and data management specifics of new studies and forms; may assist with tabulating and reviewing data results for publication and reporting.
- Also assists in developing grant applications, developing and managing budgets, subcontracts, and expenditures.
- Provides for training and orientation to research and grant procedures.
- Coordinates work schedule, monitors adherence to procedures/protocols.
- Provides input into development of performance evaluation for non-clinical aspects of staff assigned to project.
- Recommends corrective action as appropriate.
- May organize and implement aspects of research protocols and assist in coordinating clinical research projects, which may include: record review, establishing and maintaining research records, and entering data into computerized database.
- Assists research investigators in budgeting and managing financial accounts effectively within the guidelines and policies established by the Hospital as well as sponsoring agencies.
- Resolves problems and monitors monthly expense reports for accuracy and conformance to budget.
- Addresses variances as required to meet the grant budget.
- May prepare special analyses as appropriate.
- Coordinates all required submissions related to protocol, physicians and procedures to the protocol office – regulatory affairs.
- Coordinates collaborative work with other investigators and/or sites.
- Also coordinates audits and on-site visits by the pharmaceutical companies and any other appropriate groups.
- Maintains quality assurance, safety, environmental and infection control in accordance with established hospital department policies and objectives.
- Coordinates and/or conducts annual training in these areas.
- May require outside travel to evaluate sites or for other grant-related reasons.
- Maintains and enhances professional expertise through educational opportunities and review of pertinent literature.
MINIMUM QUALIFICATIONS
BASIC KNOWLEDGE: Masters Degree in relevant discipline or occupation is preferred. May consider relevant education and/or work experience year for year for degree. Excellent computer skills and familiarity with statistics. May require valid driver’s license where grant requires travel outside of hospital.
Experience: Three or more years progressively more responsible relevant experience, depending on size and complexity of program(s) or organization. Experience should demonstrate leadership skills and ability to effectively prepare and monitor budgets.
WORK ENVIRONMENT AND PHYSICAL REQUIREMENTS: While most duties are performed in an office environment, incumbent is exposed to patient care environment. Any risk of exposure to contagious or noxious elements is minimized by adherence to safety procedures and protocols.
INDEPENDENT ACTION: Incumbent functions independently within a broad scope of department policies and practices; generally refers specific problems to supervisor only where clarification of department policies and procedures may be required.
SUPERVISORY RESPONSIBILITY: May provide direct supervision for up to 3 full-time equivalent personnel assigned to the program.
Pay Range
$64,480.00-$106,412.80
Location
The Miriam Hospital - 164 Summit Ave Providence, Rhode Island 02906
Work Type
M-F 8am - 4:30pm
Work Shift
Day
Daily Hours
8 hours
Driving Required
No
Brown University Health is committed to providing equal employment opportunities and maintaining a work environment free from all forms of unlawful discrimination and harassment.
Clinical Research Job Roles in Rhode Island
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Search Clinical Research Jobs in Rhode IslandClinical Research Jobs in Rhode Island: Frequently Asked Questions
Which companies sponsor visas for clinical research roles in Rhode Island?
Lifespan Health System, Care New England, and Brown University are among the most active sponsors of international clinical research talent in Rhode Island. Smaller contract research organizations and biotech firms operating out of the Providence area also file H-1B petitions for roles such as clinical research coordinator, research analyst, and clinical data manager. Checking OFLC disclosure data confirms which employers have recent sponsorship history.
Which visa types are most common for clinical research roles in Rhode Island?
The H-1B is the most common visa for clinical research professionals in Rhode Island, covering roles like clinical research coordinator and biostatistician that meet the specialty occupation standard. J-1 visas are also prevalent for researchers affiliated with Brown University or hospital-based training programs. International graduates on OPT or STEM OPT often transition into H-1B sponsorship through Rhode Island's academic medical centers.
Which cities in Rhode Island have the most clinical research sponsorship jobs?
Providence is by far the primary hub for clinical research sponsorship jobs in Rhode Island, driven by Brown University's Warren Alpert Medical School, Rhode Island Hospital, and Women & Infants Hospital. Pawtucket and East Providence have a smaller but present concentration of research activity tied to nearby health systems. Given Rhode Island's size, most sponsored clinical research positions are realistically commutable from anywhere in the state.
How to find clinical research visa sponsorship jobs in Rhode Island?
Migrate Mate filters job listings specifically by visa sponsorship availability, making it straightforward to find clinical research roles in Rhode Island without sifting through positions that don't offer sponsorship. You can search by role type, such as clinical research coordinator or clinical data manager, and narrow results to Rhode Island employers. This saves significant time compared to reviewing unfiltered listings where sponsorship status is often unclear.
Are there any state-specific considerations for clinical research visa sponsorship in Rhode Island?
Rhode Island's clinical research hiring is closely tied to its academic medical infrastructure, so many sponsored roles require affiliation with or referral from Brown University's research network. Employers must meet DOL prevailing wage requirements for the specific role and location, which are set at the Providence-Warwick metro level for most positions. Rhode Island's compact geography also means that clinical research professionals often work across multiple affiliated hospital campuses under a single sponsorship arrangement.
What is the prevailing wage for sponsored clinical research jobs in Rhode Island?
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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