Clinical Research Visa Sponsorship Jobs in Connecticut
Connecticut's clinical research sector is anchored by Yale School of Medicine and Yale New Haven Health in New Haven, Boehringer Ingelheim in Ridgefield, and a growing cluster of biotechnology and pharmaceutical employers along the I-95 corridor. International candidates with backgrounds in clinical trials, regulatory affairs, or biostatistics will find active sponsorship activity across both academic medical centers and industry sponsors.
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Northwell is the largest not-for-profit health system in the Northeast, serving residents of New York and Connecticut with 28 hospitals, more than 1,000 outpatient facilities, 22,000 nurses and over 20,000 physicians. Northwell cares for more than three million people annually in the New York metro area, including Long Island, the Hudson Valley, Connecticut and beyond, thanks to philanthropic support from our communities. Northwell is New York State’s largest private employer with over 104,000 employees — including members of Northwell Health Physician Partners — who are working to change health care for the better.
Title: Clinical Research Coordinator - Norwalk Hospital Cancer Research, 34 Maple Ave, Norwalk, CT - Full time/40 hours per week, 8-hour shifts, 8:30am - 5:00pm, Monday - Friday.
Summary: Collaborates with departmental leadership and research staff in the coordination of all aspects of clinical research studies. Responsibilities include: patient screening and recruitment, coordination of care of the research patient, protocol implementation, data collection and query resolution, and submission to the Institutional Review Board (IRB). Coordinates studies in Oncology therapeutic areas. Functions independently in a clinical research setting and responsible for the complete coordination of assigned clinical research protocols from national research agencies and pharmaceutical corporations.
Responsibilities:
- Screens patients for study participation e.g. reviews medical record, collaborates with medical & research staff, etc. and procures informed consent.
- Maintains accurate and thorough documentation on all source documents and case report forms (CRFs) for each study patient. Resolves all patient queries.
- Maintains communication with investigators/researchers, patients, internal and external collaborators (e.g. consulting physicians), sponsors, federal regulatory agencies, and other involved parties as required.
- Participates in investigator, coordinator, or study initiation meetings accordingly. Coordinates and participates in monitoring visits/audits with regulatory agencies or sponsors.
- Maintains current regulatory (GCP, HSR) and study specific required trainings.
- Prepares and submits all study protocols, consent forms, and other required documents to the Institutional Review Board (IRB).
- Educates hospital staff about protocols through in-services, written materials and one-on-one interaction, for each study and each patient, and for general marketing.
- Demonstrates flexibility in daily routine and effectively accommodates for the needs of the job (e.g. early or late patient enrollment).
- Performs procedures including EKG, Phlebotomy, blood and body fluid sampling, packing and shipment of human samples, body measurements and examinations within scope of practice and training, consistent with clinic and study specific policies/procedures and scope of care under the guidance of the supervisor.
- Fulfills all compliance responsibilities related to the position.
- Maintain and Model Nuvance Health Values.
- Demonstrates regular, reliable and predictable attendance.
- Performs other duties as required.
Education and Experience Requirements:
- Bachelor's degree or
- Allied Health Professional Degree AND three years job-related experience.
- Minimum 1-year clinical experience in medical field.
- Prefer: Clinical Research experience
Minimum Knowledge, Skills and Abilities Requirements:
- Fluency in medical terminology.
- Knowledge of clinical trials, research and general medicine. Strong computer skills.
- Strong attention to detail and organizational skills
- Outstanding interpersonal skills
License, Registration, or Certification Requirements:
- Basic Life Support current or willing to take course
- Valid Driver’s license
- Prefer: Professional research certification
- Prefer: Basic Life Support
Salary Range: $29.65 - $55.55 hourly (Pay based on years of relative experience)
Description
Northwell is the largest not-for-profit health system in the Northeast, serving residents of New York and Connecticut with 28 hospitals, more than 1,000 outpatient facilities, 22,000 nurses and over 20,000 physicians. Northwell cares for more than three million people annually in the New York metro area, including Long Island, the Hudson Valley, Connecticut and beyond, thanks to philanthropic support from our communities. Northwell is New York State’s largest private employer with over 104,000 employees — including members of Northwell Health Physician Partners — who are working to change health care for the better.
Title: Clinical Research Coordinator - Norwalk Hospital Cancer Research, 34 Maple Ave, Norwalk, CT - Full time/40 hours per week, 8-hour shifts, 8:30am - 5:00pm, Monday - Friday.
Summary: Collaborates with departmental leadership and research staff in the coordination of all aspects of clinical research studies. Responsibilities include: patient screening and recruitment, coordination of care of the research patient, protocol implementation, data collection and query resolution, and submission to the Institutional Review Board (IRB). Coordinates studies in Oncology therapeutic areas. Functions independently in a clinical research setting and responsible for the complete coordination of assigned clinical research protocols from national research agencies and pharmaceutical corporations.
Responsibilities:
- Screens patients for study participation e.g. reviews medical record, collaborates with medical & research staff, etc. and procures informed consent.
- Maintains accurate and thorough documentation on all source documents and case report forms (CRFs) for each study patient. Resolves all patient queries.
- Maintains communication with investigators/researchers, patients, internal and external collaborators (e.g. consulting physicians), sponsors, federal regulatory agencies, and other involved parties as required.
- Participates in investigator, coordinator, or study initiation meetings accordingly. Coordinates and participates in monitoring visits/audits with regulatory agencies or sponsors.
- Maintains current regulatory (GCP, HSR) and study specific required trainings.
- Prepares and submits all study protocols, consent forms, and other required documents to the Institutional Review Board (IRB).
- Educates hospital staff about protocols through in-services, written materials and one-on-one interaction, for each study and each patient, and for general marketing.
- Demonstrates flexibility in daily routine and effectively accommodates for the needs of the job (e.g. early or late patient enrollment).
- Performs procedures including EKG, Phlebotomy, blood and body fluid sampling, packing and shipment of human samples, body measurements and examinations within scope of practice and training, consistent with clinic and study specific policies/procedures and scope of care under the guidance of the supervisor.
- Fulfills all compliance responsibilities related to the position.
- Maintain and Model Nuvance Health Values.
- Demonstrates regular, reliable and predictable attendance.
- Performs other duties as required.
Education and Experience Requirements:
- Bachelor's degree or
- Allied Health Professional Degree AND three years job-related experience.
- Minimum 1-year clinical experience in medical field.
- Prefer: Clinical Research experience
Minimum Knowledge, Skills and Abilities Requirements:
- Fluency in medical terminology.
- Knowledge of clinical trials, research and general medicine. Strong computer skills.
- Strong attention to detail and organizational skills
- Outstanding interpersonal skills
License, Registration, or Certification Requirements:
- Basic Life Support current or willing to take course
- Valid Driver’s license
- Prefer: Professional research certification
- Prefer: Basic Life Support
Salary Range: $29.65 - $55.55 hourly (Pay based on years of relative experience)
Clinical Research Job Roles in Connecticut
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Search Clinical Research Jobs in ConnecticutClinical Research Jobs in Connecticut: Frequently Asked Questions
Which companies sponsor visas for clinical research professionals in Connecticut?
Yale New Haven Health System, Yale School of Medicine, and Boehringer Ingelheim are among the most consistent sponsors for clinical research roles in Connecticut. Pfizer maintains a presence in the state, and several contract research organizations operating along the I-95 corridor have also filed H-1B visa petitions for clinical research associates, coordinators, and data managers. Sponsorship activity is concentrated in both academic medical and pharmaceutical industry settings.
Which visa types are most common for clinical research roles in Connecticut?
The H-1B is the most common visa for clinical research professionals in Connecticut, covering roles such as clinical research coordinator, biostatistician, and regulatory affairs specialist that typically require a bachelor's or advanced degree in a relevant science or health field. J-1 visas are also used for research scholars at Yale and UConn Health. Candidates with Canadian or Mexican citizenship may qualify for TN visa status under the scientist or pharmacist categories depending on their specific role.
Which cities in Connecticut have the most clinical research sponsorship jobs?
New Haven has the highest concentration of clinical research sponsorship activity in Connecticut, driven by Yale University's extensive research programs and Yale New Haven Health. Farmington is home to UConn Health, which regularly supports international researchers. Ridgefield hosts Boehringer Ingelheim's U.S. operations and generates sponsorship demand for clinical and regulatory roles. Stamford and Hartford also see activity from pharmaceutical companies and hospital systems with active research programs.
How to find clinical research visa sponsorship jobs in Connecticut?
Migrate Mate filters clinical research jobs in Connecticut specifically by visa sponsorship availability, so you're not sorting through roles that won't support international candidates. The platform surfaces positions from academic medical centers, pharmaceutical companies, and contract research organizations across New Haven, Farmington, and Ridgefield. Filtering by role type within Migrate Mate helps narrow results to clinical trial management, biostatistics, and regulatory affairs openings with confirmed sponsorship intent.
Are there any Connecticut-specific considerations for clinical research visa sponsorship candidates?
Connecticut falls under the Department of Labor's Northeast region for prevailing wage determinations, which affects the wage levels employers must certify on Labor Condition Applications for H-1B positions. Candidates targeting academic roles at Yale or UConn Health should be aware that university-affiliated positions are often cap-exempt for H-1B purposes, meaning sponsorship can proceed outside the annual lottery. Strong ties to Connecticut's university pipeline, particularly from Yale's public health and biostatistics programs, can also shape which roles receive consistent sponsorship support.
What is the prevailing wage for sponsored clinical research 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.