Clinical Research Coordinator Jobs in USA with Visa Sponsorship
There are 1,115+ clinical research coordinator positions currently offering visa sponsorship in the United States. The most common visa types for these roles include H-1B, F-1 OPT, Green Card. Top hiring companies include Beth Israel Lahey Health, University of California, San Francisco, & University of Utah, among others. Salaries for sponsored positions range from $30K – $44K.
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INTRODUCTION
Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission. As a not-for-profit, we support patient care, research, teaching, and community service, striving to provide exceptional care. We believe that high-performing teams drive groundbreaking medical discoveries and invite all applicants to join us and experience what it means to be part of Mass General Brigham.
JOB SUMMARY
The MGH Center for Health Outcomes and Interdisciplinary Research (CHOIR) within the Department of Psychiatry is seeking a Clinical Research Coordinator (CRC). CHOIR is an interdisciplinary clinical research center with a longstanding commitment to developing and testing psychosocial interventions for patients, caregivers, and patient-caregiver dyads in both hospital and community settings. CHOIR is an established center with multiple NIH-funded clinical trials, an internship in Clinical Psychology, a T32 postdoctoral fellowship, and a Resource Center for Minority Aging Research.
The CRC will assist Dr. Alexander Presciutti on two interventional studies with patients and their caregivers adjusting to critical illness (severe brain injury and cardiac arrest). They will collaborate with other members of the research team, faculty, and staff within CHOIR, but will also be expected to take initiative and work well independently. Due to the time- or deadline-sensitive nature of the projects, the CRC is expected to dynamically manage priorities. The working hours are typically 8:30-5pm. However, some tasks may fall outside of these hours due to patient scheduling.
This is a mentored position that offers valuable research experience in clinical psychology, caregiver support, neurocritical care, and interdisciplinary collaborations. This is an ideal position for people looking to apply to graduate school in clinical psychology, public health, social work, or medical school. The successful candidate will enjoy faculty and departmental support preparing graduate school applications and have the opportunity to strengthen those applications through earned co-authorships and conference presentations of scholarly research.
Further details on the two studies are below:
The CRC will spend the majority of their time leading the Coma Family Program study (COMA-F). COMA-F is a multi-site efficacy trial that will examine if a resilience intervention care reduce emotional distress among caregivers of patients with severe acute brain injury. The study will enroll 150 caregivers from three neurosciences intensive care units and associated stepdown units in the United States (Massachusetts General Hospital [MGH], University of North Carolina, and the University of Maryland Baltimore). Eligible caregiver participants are those of patients admitted with severe acute brain injury leading to coma for at least 24 hours and have committed the patient to life-sustaining therapy. The MGH CRC will be the primary CRC on the project and recruit caregivers locally at MGH.
The CRC will spend the minority of their time assisting with the Recovering Together after Cardiac Arrest study (RT-CA). RT-CA is a single-site trial examining the feasibility of a resilience intervention for cardiac arrest survivors and their caregivers. Recruitment occurs in intensive care units and associated stepdown units across the hospital.
For both studies, prior work with patients with serious illness and/or their caregivers is preferred, but not required. The CRC will be responsible for coordinating and carrying out study activities; recruiting, consenting, enrolling, and retaining participants in the study; performing study assessments and follow-ups; completing data entry and management; updating study records and documents; acting as a study resource for participants; and corresponding with CRCs from the University of North Carolina and the University of Maryland as they refer caregivers to the MGH team. They will work alongside other CRCs at CHOIR through team research meetings, trainings, and presentations led by staff within CHOIR. Competitive applicants for this position are eager to learn, take initiative, organized, conscientious, and excited to work in a close-knit team. As mentioned above, our ideal candidate has prior experience in working with patients with serious illness and/or their caregivers. Candidates from diverse backgrounds are strongly encouraged to apply.
Please submit a cover letter outlining your interests, reasons why you are a good fit for the two studies, and prior relevant experiences. We will not consider applications without a cover letter included.
PRINCIPAL DUTIES AND RESPONSIBILITIES:
- Patient screening and recruitment (in person in intensive care units and associated stepdown units, and remotely by phone or Zoom)
- Recruit and gather data from study participants (in-person and remotely).
- Correspond with other site CRCs to receive participant referrals.
- Patient follow-up.
- Maintain records and databases.
- Administer surveys to participants through electronic surveys (REDCap).
- Conduct literature and library searches.
- Ensure compliance with federal and IRB regulations.
- Assist with IRB submissions, amendments, and continuing reviews.
- Assist with preparation of grant applications and manuscripts, including data analyses, literature searches and drafting of texts.
- Perform administrative support duties as required.
- Attend individual and team meetings.
- Maintain contact and follow-up with study team members, including national recruitment sites and advisory board members.
BASIC QUALIFICATIONS:
Bachelors required
Can this role accept experience in lieu of a degree? No
QUALIFICATIONS AND EDUCATION:
Bachelor's Degree Related Field of Study required
Can this role accept experience in lieu of a degree? Yes
Experience:
Some relevant research project work 0-1 year preferred
SKILLS / ABILITIES / COMPETENCIES REQUIRED:
The candidate should:
- Be eager to learn and take initiative.
- Be well-organized, conscientious, self-motivated, and attentive to detail.
- Be able to problem-solve, function in a fast-paced environment, and manage time/work-load with minimal supervision.
- Have excellent interpersonal communication skills to effectively communicate with a multidisciplinary team and research participants.
The CRC should be proficient in using administrative software (Excel, Word, Access, PowerPoint). Experience with webpage development, patient interaction, and IRB will provide the candidate with an advantage.
WORKING CONDITIONS:
Availability to work in-person 4 out of 5 days a week are required. The working hours are typically 8:30-5pm, however, some tasks may include evening and/or weekend work due to patient scheduling.
SUPERVISORY RESPONSIBILITY: N/A
FISCAL RESPONSIBILITY: N/A
ADDITIONAL JOB DETAILS (IF APPLICABLE)
REMOTE TYPE: Hybrid
WORK LOCATION: 15 New Chardon Street
SCHEDULED WEEKLY HOURS: 40
EMPLOYEE TYPE: Regular
WORK SHIFT: Day (United States of America)
PAY RANGE: $20.16 - $29.01/Hourly
GRADE: 5
At Mass General Brigham, we believe in recognizing and rewarding the unique value each team member brings to our organization. Our approach to determining base pay is comprehensive, and any offer extended will take into account your skills, relevant experience if applicable, education, certifications and other essential factors. The base pay information provided offers an estimate based on the minimum job qualifications; however, it does not encompass all elements contributing to your total compensation package. In addition to competitive base pay, we offer comprehensive benefits, career advancement opportunities, differentials, premiums and bonuses as applicable and recognition programs designed to celebrate your contributions and support your professional growth. We invite you to apply, and our Talent Acquisition team will provide an overview of your potential compensation and benefits package.
EEO STATEMENT:
1200 The General Hospital Corporation is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religious creed, national origin, sex, age, gender identity, disability, sexual orientation, military service, genetic information, and/or other status protected under law. We will ensure that all individuals with a disability are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. To ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Veteran’s Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact Human Resources at (857)-282-7642.
MASS GENERAL BRIGHAM COMPETENCY FRAMEWORK
At Mass General Brigham, our competency framework defines what effective leadership “looks like” by specifying which behaviors are most critical for successful performance at each job level. The framework is comprised of ten competencies (half People-Focused, half Performance-Focused) and are defined by observable and measurable skills and behaviors that contribute to workplace effectiveness and career success. These competencies are used to evaluate performance, make hiring decisions, identify development needs, mobilize employees across our system, and establish a strong talent pipeline.

How to Get Visa Sponsorship as a Clinical Research Coordinator
Target CROs with large-scale global trial operations
Major CROs like IQVIA, Parexel, and ICON manage thousands of clinical trials and hire CRCs across dozens of U.S. sites. Their scale means they have dedicated immigration teams and experience filing visa petitions for research staff. Apply to their U.S. operations specifically, as these tend to have the most sponsorship activity.
Earn your CCRC or CCRP certification early
Getting certified through ACRP or SoCRA demonstrates specialized knowledge of FDA regulations and Good Clinical Practice guidelines. Certification strengthens your H-1B petition by establishing clinical research as a distinct professional discipline. You can begin studying and sit for the exam while on OPT.
Gain experience in high-demand therapeutic areas
Oncology, rare diseases, and cell and gene therapy trials are expanding rapidly and face coordinator shortages. CRCs with experience in these complex therapeutic areas are harder to replace, which strengthens the case for sponsorship. Highlight specific protocol experience and any specialized training you have completed.
Learn clinical trial management systems thoroughly
Expertise in CTMS platforms like Medidata Rave, Oracle Clinical, or Veeva Vault is increasingly required for CRC positions. Knowing how to manage electronic data capture (EDC), regulatory document tracking, and site management tools makes you operationally essential. This technical proficiency differentiates you from coordinators who rely solely on paper-based processes.
Look for academic medical center positions
University-affiliated hospitals and research centers - such as those at Johns Hopkins, UCSF, and Mayo Clinic - often have cap-exempt H-1B status for research-related roles. CRC positions tied to federally funded clinical trials at these institutions may qualify. Cap-exempt means no lottery and the ability to file year-round.
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Get Access To All JobsFrequently Asked Questions
Do pharmaceutical companies and CROs sponsor visas for clinical research coordinators?
Yes, large contract research organizations (CROs) like IQVIA, Parexel, ICON, and Syneos Health hire clinical research coordinators and may sponsor H-1B visas for candidates with the right qualifications. Pharmaceutical sponsors such as Pfizer, Merck, and Roche also hire CRCs at their clinical trial sites. A bachelor's degree in a life science or health-related field is typically required for sponsorship eligibility.
What certifications help clinical research coordinators get sponsored?
The CCRC (Certified Clinical Research Coordinator) from ACRP and the CCRP (Certified Clinical Research Professional) from SoCRA are the two most recognized certifications in the field. Either certification demonstrates specialized knowledge of FDA regulations, Good Clinical Practice (GCP), and trial management. Having one can differentiate you from candidates without formal clinical research credentials.
Is clinical research coordination eligible for STEM OPT?
STEM OPT eligibility depends on your degree program's CIP code, not your job title. If your degree is in biology, biomedical science, public health (biostatistics), or another STEM-classified field, you may qualify for the 24-month extension. This gives you up to 36 months of work authorization to build your track record before H-1B filing.
Can clinical research coordinators transition to higher-level roles that are easier to sponsor?
Absolutely. CRC experience is a stepping stone to clinical research manager, clinical operations lead, or clinical project manager roles at CROs and pharma companies. These senior positions typically have higher salaries and more clearly defined specialty occupation requirements, which can make H-1B petitions more straightforward. Many CRCs also move into regulatory affairs or medical science liaison roles.
What is the prevailing wage requirement for sponsored Clinical Research Coordinator jobs?
When a U.S. employer sponsors a foreign worker for a work visa, they are legally required to pay at least the "prevailing wage" — the average wage paid to workers in the same occupation, in the same geographic area, with similar experience. This is set by the Department of Labor to prevent employers from hiring foreign workers at below-market rates. The prevailing wage varies significantly by role, location, and experience level — for example, a clinical research coordinator in Massachusetts will have a different prevailing wage than the same role in a smaller state. You can look up current prevailing wage rates for any occupation and location using the OFLC Wage Search.
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