Clinical Research Scientist Jobs in USA with Visa Sponsorship
Clinical Research Scientists work in specialty occupations that qualify for H-1B visa, O-1, and EB-2 NIW sponsorship. Most roles require a master's or doctoral degree in a life sciences field. Employers including pharmaceutical companies, CROs, and academic medical centers regularly sponsor qualified candidates. For detailed occupation requirements, see the O*NET profile.
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Get Access To All JobsCOMPANY DESCRIPTION
Artech Information Systems is the #12 Largest IT Staffing Company in the U.S. and an employer of choice for over 7,000 consultants. We recruit world-class talent for IT, engineering, and other professional jobs at 70+ Fortune and Global 500 companies coast-to-coast across the U.S., India, and China. We are one of the fastest-growing companies in the US and we welcome you to search the thousands of jobs in our cutting-edge GEM system for employment opportunities that fit your qualifications.
At the forefront of the staffing industry, Artech is a minority and women-owned business enterprise (MWBE) committed to maximizing global workforce solutions on behalf of its clients. Artech's deep heritage, proven expertise and insightful market intelligence has secured long-term partnerships with Fortune 500 and government clients seeking world-class professional resources.
JOB DESCRIPTION
The incumbent is responsible for, but not limited to the following:
- Assist in the planning, implementation, managing, and reporting of Phase I-III clinical studies
- Prepare and review project and study documents including clinical trial protocols, clinical study reports, patient SAE narratives, clinical sections of registration dossier documents (ISS, Client, Investigator Brochure, etc)
- Performs literature search and data analysis to address research questions
- In collaboration with other clinical staff and/or an external CRO, monitoring clinical trial conduct (enrollment, GCP practices, handling of safety issues, etc.)
- Assisting in database cleaning, review of study results, and interpretation of results
- Adhering to key performance indicators for clinical study development, conduct, and reporting
- Individual contributor with specialized knowledge
- Presents concepts, facts, and reports and advises on key trends and issues
- Troubleshooting routine site inquiries
- Work is completed under limited supervision
- Supports the planning, execution and reporting of clinical programs/trials
- May handle multiple protocols simultaneously
- Contributes to risk resolution by escalating and monitoring project risks
- Minimum of 5-7 years of experience in clinical research in the pharmaceutical industry
- A thorough understanding of clinical research methodology including study design, protocol writing, and CRF preparation is required, as is a knowledge of GCP and local regulatory requirements
- Working knowledge of the IND/NDA/CTD/MAA process acquired through direct industrial experience preferred
- Knowledge of medical, scientific and clinical research techniques in the oncology therapeutic area
- Bachelor's Required. Doctoral (PharmD or PhD) degree preferred
QUALIFICATIONS
BS/MS
ADDITIONAL INFORMATION
For more information, Please contact
Best Regards,
Akriti Gupta
(973) 967-3409
Morristown, NJ 07960
COMPANY DESCRIPTION
Artech Information Systems is the #12 Largest IT Staffing Company in the U.S. and an employer of choice for over 7,000 consultants. We recruit world-class talent for IT, engineering, and other professional jobs at 70+ Fortune and Global 500 companies coast-to-coast across the U.S., India, and China. We are one of the fastest-growing companies in the US and we welcome you to search the thousands of jobs in our cutting-edge GEM system for employment opportunities that fit your qualifications.
At the forefront of the staffing industry, Artech is a minority and women-owned business enterprise (MWBE) committed to maximizing global workforce solutions on behalf of its clients. Artech's deep heritage, proven expertise and insightful market intelligence has secured long-term partnerships with Fortune 500 and government clients seeking world-class professional resources.
JOB DESCRIPTION
The incumbent is responsible for, but not limited to the following:
- Assist in the planning, implementation, managing, and reporting of Phase I-III clinical studies
- Prepare and review project and study documents including clinical trial protocols, clinical study reports, patient SAE narratives, clinical sections of registration dossier documents (ISS, Client, Investigator Brochure, etc)
- Performs literature search and data analysis to address research questions
- In collaboration with other clinical staff and/or an external CRO, monitoring clinical trial conduct (enrollment, GCP practices, handling of safety issues, etc.)
- Assisting in database cleaning, review of study results, and interpretation of results
- Adhering to key performance indicators for clinical study development, conduct, and reporting
- Individual contributor with specialized knowledge
- Presents concepts, facts, and reports and advises on key trends and issues
- Troubleshooting routine site inquiries
- Work is completed under limited supervision
- Supports the planning, execution and reporting of clinical programs/trials
- May handle multiple protocols simultaneously
- Contributes to risk resolution by escalating and monitoring project risks
- Minimum of 5-7 years of experience in clinical research in the pharmaceutical industry
- A thorough understanding of clinical research methodology including study design, protocol writing, and CRF preparation is required, as is a knowledge of GCP and local regulatory requirements
- Working knowledge of the IND/NDA/CTD/MAA process acquired through direct industrial experience preferred
- Knowledge of medical, scientific and clinical research techniques in the oncology therapeutic area
- Bachelor's Required. Doctoral (PharmD or PhD) degree preferred
QUALIFICATIONS
BS/MS
ADDITIONAL INFORMATION
For more information, Please contact
Best Regards,
Akriti Gupta
(973) 967-3409
Morristown, NJ 07960
See all 925+ Clinical Research Scientist jobs
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Clinical Research Scientist roles.
Get Access To All JobsTips for Finding Visa Sponsorship as a Clinical Research Scientist
Target CROs and pharma sponsors first
Contract research organizations and large pharmaceutical companies have established immigration infrastructure and sponsor Clinical Research Scientists routinely. These employers process H-1B petitions far more efficiently than smaller biotech startups or academic departments new to sponsorship.
Confirm your degree field matches the role
H-1B specialty occupation requires a direct nexus between your degree field and the job duties. A degree in clinical pharmacology, biostatistics, or epidemiology maps cleanly. A general biology degree may require additional documentation to satisfy USCIS specialty occupation standards.
Register for the H-1B lottery by March
USCIS opens H-1B registration in early March each year. Your employer must register you before the deadline. Missing it means waiting a full year. Confirm your employer's immigration counsel has you registered before the window closes.
Consider the O-1A if you have published research
Clinical Research Scientists with peer-reviewed publications, conference presentations, or significant trial leadership may qualify for the O-1A extraordinary ability visa. This bypasses the lottery entirely and is worth discussing with an immigration attorney before assuming H-1B is your only path.
EB-2 NIW is viable if your research has national impact
If your clinical research addresses public health priorities or rare disease areas, you may self-petition for an EB-2 National Interest Waiver without employer sponsorship. This is particularly relevant for researchers working in oncology, infectious disease, or neglected conditions.
Get the LCA details in writing before accepting an offer
Ask your employer to confirm the prevailing wage level on the Labor Condition Application before you sign. The LCA wage level directly affects your H-1B petition and sets the floor for what you must be paid throughout the sponsorship period.
Clinical Research Scientist jobs are hiring across the US. Find yours.
Find Clinical Research Scientist JobsFrequently Asked Questions
Do Clinical Research Scientist roles qualify as H-1B specialty occupations?
Yes. Clinical Research Scientist positions consistently qualify as H-1B specialty occupations because the role normally requires at minimum a bachelor's degree in a specific scientific field such as clinical pharmacology, biochemistry, or biostatistics. USCIS has a strong approval history for this title across pharmaceutical and academic medical employers, though job duty documentation matters.
What degree do I need for a Clinical Research Scientist to sponsor my H-1B?
Most employers require a master's degree or Ph.D. in a life sciences field for Clinical Research Scientist roles, though some entry-level positions accept a bachelor's degree with substantial clinical trial experience. USCIS requires the degree field to directly relate to the job duties, so a degree in clinical research, pharmacology, epidemiology, or a closely related discipline is strongest.
Which employers most commonly sponsor Clinical Research Scientists?
The largest H-1B sponsors for this role are major pharmaceutical companies, large contract research organizations, and academic medical centers with active clinical trial programs. These employers have in-house immigration teams and sponsor researchers regularly. You can browse open Clinical Research Scientist roles from verified sponsoring employers on Migrate Mate.
Can I qualify for an EB-2 National Interest Waiver as a Clinical Research Scientist?
Potentially, yes. The NIW is well-suited for clinical researchers whose work addresses public health challenges with national significance, such as oncology trials, infectious disease research, or studies targeting rare conditions. You must show your work has substantial merit, national scope, and that waiving the job offer requirement serves U.S. interests. An immigration attorney can assess your publication and trial record.
What happens to my H-1B sponsorship if my clinical trial project ends mid-petition?
Your H-1B status is tied to the employer, not the specific project. As long as your employer-employee relationship continues and your duties remain consistent with the approved petition, project transitions do not require a new filing. If your role changes significantly, your employer should file an amended H-1B petition. A gap in employment, however, can put your status at risk.
What is the prevailing wage requirement for sponsored Clinical Research Scientist jobs?
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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