Clinical Research Nurse Green Card Jobs
Clinical Research Nurse roles at academic medical centers, contract research organizations, and pharmaceutical companies qualify for EB-2 and EB-3 green card sponsorship through PERM labor certification. Employers document the hire through DOL's PERM process before filing an I-140 petition, putting you on the path to permanent residency rather than a renewable temporary status.
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Job Ref:
JR-3446
Location:
450 Brookline Ave, BOSTON, MA 02215
Category:
Nursing
Employment Type:
Full time
Work Location:
Onsite: occasional remote
Salary/Pay Rate:
$42.65 - $105.81 per hour
Overview
The Research Nurse in collaboration with the physician, is responsible for the implementation and evaluation of clinical research in their specific program/area. The CRN has expert knowledge of cancer as a disease process, cancer treatment modalities (or comparable knowledge for a non-oncology area, e.g. infection control) and the process of conducting medical clinical research. In addition, the CRN utilizes evidence-based nursing practice and has expertise in developing and coordinating a plan of care designed to meet the physical, psychological, and social needs of those cancer patients and their families undergoing therapy in a clinical research trial. Strong interpersonal, organizational and communication skills are required. Knowledge of current literature and a commitment to continued learning are also required. Specific duties and responsibilities may vary across the different programs/areas. Located in Boston and the surrounding communities, Dana-Farber Cancer Institute is a leader in life changing breakthroughs in cancer research and patient care. We are united in our mission of conquering cancer, HIV/AIDS, and related diseases. We strive to create an inclusive, diverse, and equitable environment where we provide compassionate and comprehensive care to patients of all backgrounds, and design programs to promote public health particularly among high-risk and underserved populations. We conduct groundbreaking research that advances treatment, we educate tomorrow's physician/researchers, and we work with amazing partners, including other Harvard Medical School-affiliated hospitals.
Primary Duties and Responsibilities:
Administrative:
- Assists principal investigator with protocol development.
- Assists principal investigator as appropriate with the Institute’s protocol review process.
- Assists the principal investigator in developing the protocol budget.
- Collaborates with the Dana-Farber Harvard Cancer Center DFHCC quality assurance of clinical trials office in developing protocol specific materials.
- Serves as research coordinator for National Cancer Institute, pharmaceutical-sponsored, and National Cooperative Group protocols.
Research:
- Assists with recruitment and registration of patients to clinical trials.
- Coordinates scheduling of patient’s laboratory and radiographic assessments, admissions and clinic visits.
- Monitors test results as appropriate.
- Coordinates protocol data management as necessary.
- Collaborates with staff within the Institute and with outside organizations in the completion of clinical research trials.
Clinical:
- Coordinates study enrollment, protocol treatment, and completion of study requirements for patients participating in clinical trials.
- Works collaboratively and functions as an effective member of the health care team.
- Collaborates with Care Coordination for all patient care referrals.
- Collaborates with primary nurse in assuring that patient care needs are met.
- Provides protocol education to patients and families; adapts interactions based on age-specific needs of the patient.
- Collects and prepares required specimens for analysis and monitors test results, as appropriate.
- Documents in charts as appropriate and communicates observations and findings to protocol investigator and attending physicians.
- Provides protocol in-service training and serves as a resource to the health care team.
- Monitors the environment of care with attention to patient safety, and assures compliance with regulatory agency standards.
- Maintains clinical practice that is evidence-based and consistent with nursing policies, procedures, licensure/registration requirements, and professional scope and standards.
- Participates in QA/QI projects for the clinical program and the Division of Nursing and Patient Care Services.
- Adheres to the Code of Ethics for Nurses with Interpretive Statements (ANA, 2001) in all aspects of professional practice.
- Fosters an environment that is sensitive to the needs of diverse populations, including but not limited to culture, ethnicity, gender, and age.
- Administers medications as necessary.
- Maintains BLS certification.
Professional Development:
- Identifies areas for professional growth.
- Formulates professional goals, objectives and methods for accomplishing these.
- Pursues active membership of local and national professional organizations.
- Supports research activities within the Division of Nursing and Patient Care Services.
- Participates in Division of Nursing / Institute committees.
- Meets all annual evaluation requirements and competencies within the established time period.
- Collaborates in preparing professional reports, articles, and presentations for colleagues and the public.
Minimum Job Qualifications:
Education: Associate degree, Nursing. Baccalaureate degree in Nursing strongly preferred. If Associate degree in Nursing, must complete BSN degree within 4 years.
Experience: 1 year of recent experience as a Registered Nurse. Ambulatory and/or oncology experience preferred.
License/Certification/Registration Required:
Licensed as a Registered Nurse in the Commonwealth of Massachusetts, or State of New Hampshire as appropriate required. AHA BLS required (AHA ACLS accepted as minimum requirement). Professional nursing certification preferred (OCN, BMTCN, CPHON, AOCNP, CRNI, RN-BC).
Supervisory Responsibilities:
None
Patient Contact:
Yes.
At Dana-Farber Cancer Institute, we work every day to create an innovative, caring, and inclusive environment where every patient, family, and staff member feels they belong. As relentless as we are in our mission to reduce the burden of cancer for all, we are committed to having faculty and staff who offer multifaceted experiences. Cancer knows no boundaries and when it comes to hiring the most dedicated and compassionate professionals, neither do we. If working in this kind of organization inspires you, we encourage you to apply.
Dana-Farber Cancer Institute is an equal opportunity employer and affirms the right of every qualified applicant to receive consideration for employment without regard to race, color, religion, sex, gender identity or expression, national origin, sexual orientation, genetic information, disability, age, ancestry, military service, protected veteran status, or other characteristics protected by law.
EEO Poster
Pay Transparency Statement
The hiring range is based on market pay structures, with individual salaries determined by factors such as business needs, market conditions, internal equity, and based on the candidate’s relevant experience, skills and qualifications.
For union positions, the pay range is determined by the Collective Bargaining Agreement (CBA).
$42.65 - $105.81

Job Ref:
JR-3446
Location:
450 Brookline Ave, BOSTON, MA 02215
Category:
Nursing
Employment Type:
Full time
Work Location:
Onsite: occasional remote
Salary/Pay Rate:
$42.65 - $105.81 per hour
Overview
The Research Nurse in collaboration with the physician, is responsible for the implementation and evaluation of clinical research in their specific program/area. The CRN has expert knowledge of cancer as a disease process, cancer treatment modalities (or comparable knowledge for a non-oncology area, e.g. infection control) and the process of conducting medical clinical research. In addition, the CRN utilizes evidence-based nursing practice and has expertise in developing and coordinating a plan of care designed to meet the physical, psychological, and social needs of those cancer patients and their families undergoing therapy in a clinical research trial. Strong interpersonal, organizational and communication skills are required. Knowledge of current literature and a commitment to continued learning are also required. Specific duties and responsibilities may vary across the different programs/areas. Located in Boston and the surrounding communities, Dana-Farber Cancer Institute is a leader in life changing breakthroughs in cancer research and patient care. We are united in our mission of conquering cancer, HIV/AIDS, and related diseases. We strive to create an inclusive, diverse, and equitable environment where we provide compassionate and comprehensive care to patients of all backgrounds, and design programs to promote public health particularly among high-risk and underserved populations. We conduct groundbreaking research that advances treatment, we educate tomorrow's physician/researchers, and we work with amazing partners, including other Harvard Medical School-affiliated hospitals.
Primary Duties and Responsibilities:
Administrative:
- Assists principal investigator with protocol development.
- Assists principal investigator as appropriate with the Institute’s protocol review process.
- Assists the principal investigator in developing the protocol budget.
- Collaborates with the Dana-Farber Harvard Cancer Center DFHCC quality assurance of clinical trials office in developing protocol specific materials.
- Serves as research coordinator for National Cancer Institute, pharmaceutical-sponsored, and National Cooperative Group protocols.
Research:
- Assists with recruitment and registration of patients to clinical trials.
- Coordinates scheduling of patient’s laboratory and radiographic assessments, admissions and clinic visits.
- Monitors test results as appropriate.
- Coordinates protocol data management as necessary.
- Collaborates with staff within the Institute and with outside organizations in the completion of clinical research trials.
Clinical:
- Coordinates study enrollment, protocol treatment, and completion of study requirements for patients participating in clinical trials.
- Works collaboratively and functions as an effective member of the health care team.
- Collaborates with Care Coordination for all patient care referrals.
- Collaborates with primary nurse in assuring that patient care needs are met.
- Provides protocol education to patients and families; adapts interactions based on age-specific needs of the patient.
- Collects and prepares required specimens for analysis and monitors test results, as appropriate.
- Documents in charts as appropriate and communicates observations and findings to protocol investigator and attending physicians.
- Provides protocol in-service training and serves as a resource to the health care team.
- Monitors the environment of care with attention to patient safety, and assures compliance with regulatory agency standards.
- Maintains clinical practice that is evidence-based and consistent with nursing policies, procedures, licensure/registration requirements, and professional scope and standards.
- Participates in QA/QI projects for the clinical program and the Division of Nursing and Patient Care Services.
- Adheres to the Code of Ethics for Nurses with Interpretive Statements (ANA, 2001) in all aspects of professional practice.
- Fosters an environment that is sensitive to the needs of diverse populations, including but not limited to culture, ethnicity, gender, and age.
- Administers medications as necessary.
- Maintains BLS certification.
Professional Development:
- Identifies areas for professional growth.
- Formulates professional goals, objectives and methods for accomplishing these.
- Pursues active membership of local and national professional organizations.
- Supports research activities within the Division of Nursing and Patient Care Services.
- Participates in Division of Nursing / Institute committees.
- Meets all annual evaluation requirements and competencies within the established time period.
- Collaborates in preparing professional reports, articles, and presentations for colleagues and the public.
Minimum Job Qualifications:
Education: Associate degree, Nursing. Baccalaureate degree in Nursing strongly preferred. If Associate degree in Nursing, must complete BSN degree within 4 years.
Experience: 1 year of recent experience as a Registered Nurse. Ambulatory and/or oncology experience preferred.
License/Certification/Registration Required:
Licensed as a Registered Nurse in the Commonwealth of Massachusetts, or State of New Hampshire as appropriate required. AHA BLS required (AHA ACLS accepted as minimum requirement). Professional nursing certification preferred (OCN, BMTCN, CPHON, AOCNP, CRNI, RN-BC).
Supervisory Responsibilities:
None
Patient Contact:
Yes.
At Dana-Farber Cancer Institute, we work every day to create an innovative, caring, and inclusive environment where every patient, family, and staff member feels they belong. As relentless as we are in our mission to reduce the burden of cancer for all, we are committed to having faculty and staff who offer multifaceted experiences. Cancer knows no boundaries and when it comes to hiring the most dedicated and compassionate professionals, neither do we. If working in this kind of organization inspires you, we encourage you to apply.
Dana-Farber Cancer Institute is an equal opportunity employer and affirms the right of every qualified applicant to receive consideration for employment without regard to race, color, religion, sex, gender identity or expression, national origin, sexual orientation, genetic information, disability, age, ancestry, military service, protected veteran status, or other characteristics protected by law.
EEO Poster
Pay Transparency Statement
The hiring range is based on market pay structures, with individual salaries determined by factors such as business needs, market conditions, internal equity, and based on the candidate’s relevant experience, skills and qualifications.
For union positions, the pay range is determined by the Collective Bargaining Agreement (CBA).
$42.65 - $105.81
See all 327+ Clinical Research Nurse jobs
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Clinical Research Nurse roles.
Get Access To All JobsTips for Finding Green Card Sponsorship as a Clinical Research Nurse
Verify your nursing credentials qualify for PERM
PERM requires your employer to define minimum job requirements before advertising. If your BSN and clinical research experience don't align with those posted requirements, USCIS can deny the I-140 petition. Get a formal credential evaluation before any offer is finalized.
Target employers with active PERM filing history
Academic medical centers, contract research organizations, and pharmaceutical sponsors file PERM regularly for nursing roles. Search OFLC's public disclosure data to confirm a prospective employer has certified PERM applications for Clinical Research Nurse or similar titles in the past two years.
Find green card sponsoring research employers on Migrate Mate
Migrate Mate filters jobs by employers with documented EB-2 and EB-3 sponsorship history, so you're applying to organizations already familiar with the PERM process for nursing roles rather than introducing the concept during salary negotiations.
Confirm the job description meets specialty occupation standards
EB-2 sponsorship requires the role to demand an advanced degree. Ensure your employer's posted job description specifies a BSN plus a master's or equivalent specialized experience, not just a generic nursing degree, or USCIS may classify the position as EB-3 skilled worker instead.
Ask about priority date strategy before accepting an offer
EB-3 applicants from most countries face no significant backlog, but Indian and Chinese nationals can wait years after I-140 approval. Negotiating concurrent I-485 filing, where the employer files the I-140 and you file adjustment of status simultaneously, shortens total processing time materially.
Document Good Clinical Practice certifications during the PERM period
PERM advertising must reflect the actual minimum requirements at the time of filing. If you earn additional certifications like CCRP or ICH-GCP training after the PERM is certified, those credentials support your I-140 petition but cannot retroactively change the posted job requirements.
Clinical Research Nurse jobs are hiring across the US. Find yours.
Find Clinical Research Nurse JobsClinical Research Nurse Green Card Sponsorship: Frequently Asked Questions
Does a Clinical Research Nurse role qualify for EB-2 or EB-3 green card sponsorship?
Both categories apply depending on how your employer structures the position. If the role requires a master's degree or equivalent specialized experience in clinical research, your employer can pursue EB-2. Roles requiring only a BSN typically fall under EB-3 skilled worker. Your employer's HR or immigration counsel defines the category when drafting the PERM job description, so it's worth confirming the classification before signing an offer.
How is green card sponsorship different from H-1B sponsorship for this role?
Green card sponsorship through PERM and I-140 leads to permanent residency, not a temporary status that needs renewing every two or three years. There's no annual lottery for EB-3, and most nationalities face no meaningful priority date backlog at that category. H-1B is a nonimmigrant status with a finite term and lottery risk; EB-3 green card sponsorship carries neither constraint, though PERM labor certification adds several months to the total timeline before USCIS adjudicates the I-140.
How long does the full EB-3 green card process take for a Clinical Research Nurse?
From PERM advertising through adjustment of status approval, most applicants from non-backlogged countries should budget 18 to 30 months. PERM's supervised recruitment and DOL certification alone takes roughly eight to twelve months before your employer can file the I-140 petition. USCIS then adjudicates I-140, followed by I-485 if you're adjusting status inside the United States. Premium processing is available for I-140 but not for PERM or I-485.
What should I look for when identifying employers who will sponsor a green card for this role?
Prioritize academic medical centers with dedicated clinical trial units, large contract research organizations, and pharmaceutical or biotech companies with established immigration programs. These organizations file PERM regularly and have internal processes for nursing sponsorship. Migrate Mate lets you filter job listings specifically by employers with documented EB-2 and EB-3 sponsorship history, so you're targeting organizations that have already committed to sponsoring roles like yours.
Can my employer start the PERM process while I'm working on an H-1B or OPT?
Yes, and starting early is standard practice. PERM is employer-driven and runs parallel to your current work authorization status. DOL requires the employer to advertise the position and document recruitment before certifying the application, which can take eight to twelve months before the I-140 is even filed. Beginning PERM while you're on H-1B buys significant runway before any visa renewal pressure, and your existing authorization status doesn't affect PERM eligibility or processing.
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