Biostatistician Jobs in USA with Visa Sponsorship
Biostatistician positions consistently qualify for H-1B visa, O-1 visa, and EB-2 visa sponsorship due to their specialized statistical expertise and advanced degree requirements. Most roles require an MS in biostatistics, epidemiology, or statistics, making visa approval straightforward for qualified candidates. For detailed occupation requirements, see the O*NET profile.
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Get Access To All JobsJob Title: Senior Biostatistician
Job Requisition ID: 2598
Posting Start Date: 11/11/26
At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society.
Job Summary
Position leads statistical support for low to medium complexity studies including contributing to development of optimal study design, follow and execute statistical analysis plan and helps in interpretation of results with supervision. This position contributes to specific aspects of drug development plans with supervision and contributes to documents submitted to Health Authorities globally with supervision. This position also works on statistical methodology and leads/contributes to internal statistical workstreams to address various project needs. The position works closely with contract research organization (CRO) programmers and statisticians and collaborates with internal programmers in preparing analysis files and performing statistical analyses. Additionally, this position interacts with study teams. This position works under supervision to solve complex study problems.
Responsibilities
Protocol Development, Case Report Form (CRF; review), Statistical Analysis Plan (SAP), Statistical Analysis, Results Interpretation, and clinical study report (CSR):
- Executes statistical activities for low to medium complexity studies including study design, protocol development, CRF review, SAP development, analysis files development, data surveillance review, statistical analysis accuracy validation, results interpretation and CSR input and review.
- Acts as main statistical contact for the assigned studies and projects.
- Provides guidance to study team on all aspects of statistical activities.
- Works closely with statistical programmers in statistical analyses execution, quality control, and data derivation.
- Collaborates closely with data manager to ensure high quality data.
Global strategy to Improve Drug Development:
- Primarily participates and may occasionally lead moderately complex biostatistical initiatives, with supervision, to improve the harmonization and efficiency of drug development which leads to cost savings and shortened timelines for the company.
CRO / Vendor Oversight:
- Review CRO/vendor proposal and budget. Set expectation on deliverables and timelines to guide CRO biostatistician and statistical programmers on complex studies.
- Ensures deliverables are accurate and delivered according to the timelines.
Global Health Authority Interaction / Negotiation:
- Contributes to documents submitted to Health Authorities globally by providing input for the interaction or by writing the interaction document. May participate in meeting or teleconferences with Health Authorities.
Qualifications
Education Qualifications
- Minimum 3 years experience with a Master Degree in statistics or biostatistics required.
- Minimum 0-2 years relevant experience in the pharmaceutical industry with Ph.D. in statistics or biostatistics or equivalent field. Ph.D. is strongly preferred.
Experience Qualifications
- Strong knowledge of statistical methodologies.
- Some understanding of current drug development trends and regulatory environments.
- Sufficient programming skills in SAS and/or R and working knowledge of software such as nQuery, East, etc.
- Strong analytical and problem-solving skills.
- Some knowledge of pharmacology, clinical research, and medical terminology and use it for study design and results interpretation.
- Excellent oral and written communication skills in English.
- Ability to identify and investigate issues and causes and formulate potential solutions with supervision.
- Ability to prioritize multiple tasks, develop instructions and manage vendors and collaborate with internal programming colleagues in completing the deliverables with high quality according to timelines, and provide recommendations to improve process.
- Compliant with internal and external compliance practice to ensure integrity of work and suggest innovative approaches to improve compliances and processes.
- Some knowledge of clinical trial methodologies.
Travel Requirements
- Ability to travel up to 10% of the time.
Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law.
Salary Range:
USD$122,880.00 - USD$184,320.00
Job Title: Senior Biostatistician
Job Requisition ID: 2598
Posting Start Date: 11/11/26
At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society.
Job Summary
Position leads statistical support for low to medium complexity studies including contributing to development of optimal study design, follow and execute statistical analysis plan and helps in interpretation of results with supervision. This position contributes to specific aspects of drug development plans with supervision and contributes to documents submitted to Health Authorities globally with supervision. This position also works on statistical methodology and leads/contributes to internal statistical workstreams to address various project needs. The position works closely with contract research organization (CRO) programmers and statisticians and collaborates with internal programmers in preparing analysis files and performing statistical analyses. Additionally, this position interacts with study teams. This position works under supervision to solve complex study problems.
Responsibilities
Protocol Development, Case Report Form (CRF; review), Statistical Analysis Plan (SAP), Statistical Analysis, Results Interpretation, and clinical study report (CSR):
- Executes statistical activities for low to medium complexity studies including study design, protocol development, CRF review, SAP development, analysis files development, data surveillance review, statistical analysis accuracy validation, results interpretation and CSR input and review.
- Acts as main statistical contact for the assigned studies and projects.
- Provides guidance to study team on all aspects of statistical activities.
- Works closely with statistical programmers in statistical analyses execution, quality control, and data derivation.
- Collaborates closely with data manager to ensure high quality data.
Global strategy to Improve Drug Development:
- Primarily participates and may occasionally lead moderately complex biostatistical initiatives, with supervision, to improve the harmonization and efficiency of drug development which leads to cost savings and shortened timelines for the company.
CRO / Vendor Oversight:
- Review CRO/vendor proposal and budget. Set expectation on deliverables and timelines to guide CRO biostatistician and statistical programmers on complex studies.
- Ensures deliverables are accurate and delivered according to the timelines.
Global Health Authority Interaction / Negotiation:
- Contributes to documents submitted to Health Authorities globally by providing input for the interaction or by writing the interaction document. May participate in meeting or teleconferences with Health Authorities.
Qualifications
Education Qualifications
- Minimum 3 years experience with a Master Degree in statistics or biostatistics required.
- Minimum 0-2 years relevant experience in the pharmaceutical industry with Ph.D. in statistics or biostatistics or equivalent field. Ph.D. is strongly preferred.
Experience Qualifications
- Strong knowledge of statistical methodologies.
- Some understanding of current drug development trends and regulatory environments.
- Sufficient programming skills in SAS and/or R and working knowledge of software such as nQuery, East, etc.
- Strong analytical and problem-solving skills.
- Some knowledge of pharmacology, clinical research, and medical terminology and use it for study design and results interpretation.
- Excellent oral and written communication skills in English.
- Ability to identify and investigate issues and causes and formulate potential solutions with supervision.
- Ability to prioritize multiple tasks, develop instructions and manage vendors and collaborate with internal programming colleagues in completing the deliverables with high quality according to timelines, and provide recommendations to improve process.
- Compliant with internal and external compliance practice to ensure integrity of work and suggest innovative approaches to improve compliances and processes.
- Some knowledge of clinical trial methodologies.
Travel Requirements
- Ability to travel up to 10% of the time.
Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law.
Salary Range:
USD$122,880.00 - USD$184,320.00
See all 658+ Biostatistician Jobs
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Biostatistician roles.
Get Access To All JobsTips for Finding Biostatistician Jobs
Target pharmaceutical and biotech companies
Major pharma companies like Pfizer, Johnson & Johnson, and Moderna regularly sponsor biostatisticians. Their established immigration departments make the H-1B process smoother than smaller organizations.
Emphasize regulatory compliance expertise
FDA submission experience and knowledge of GCP/ICH guidelines strengthen your specialty occupation case. Mention specific statistical software proficiency like SAS, R, or STATA in applications.
Consider CRO alternatives to direct pharma
Contract research organizations like IQVIA, PPD, and Syneos Health hire extensively and often have more flexible sponsorship policies than traditional pharmaceutical companies.
Leverage academic medical center opportunities
Research hospitals and university medical centers frequently sponsor biostatisticians for clinical trials. These positions may qualify for cap-exempt H-1B filing, avoiding the lottery entirely.
Highlight clinical trial methodology experience
Experience with randomized controlled trials, adaptive designs, and survival analysis demonstrates the specialized knowledge required for visa approval. Document specific therapeutic areas you've supported.
Consider the EB-2 NIW pathway early
Biostatisticians with publications in peer-reviewed journals may qualify for National Interest Waiver green cards. This bypasses employer sponsorship requirements and labor certification processes.
Frequently Asked Questions
Do biostatistician roles qualify for H-1B visa sponsorship?
Yes, biostatistician positions consistently qualify for H-1B visa sponsorship because they require specialized statistical knowledge and typically mandate a master's degree in biostatistics, epidemiology, or statistics. The role's focus on clinical trial design and regulatory compliance clearly meets specialty occupation requirements.
How to find Biostatistician jobs with visa sponsorship?
To find Biostatistician jobs with visa sponsorship, use Migrate Mate, which specializes in connecting international professionals with sponsoring employers. Focus on pharmaceutical companies, clinical research organizations, and biotech firms that commonly offer H-1B, O-1, or TN visas for statistical roles. These employers frequently need biostatisticians for drug development, clinical trials, and regulatory submissions, making them more likely to sponsor qualified international candidates.
What degree do I need for visa sponsorship as a biostatistician?
Most employers require a master's degree in biostatistics, statistics, epidemiology, or a related quantitative field. A bachelor's in mathematics or statistics plus extensive clinical research experience may qualify, but the master's degree significantly strengthens your sponsorship case with USCIS.
Which visa types work best for biostatistician positions?
H-1B is the most common pathway, with pharmaceutical companies regularly sponsoring biostatisticians. O-1 visas suit candidates with exceptional research records and publications. EB-2 green cards work well for senior biostatisticians, especially through the National Interest Waiver route for those with significant contributions to public health.
Do pharmaceutical companies sponsor international biostatisticians?
Yes, major pharmaceutical companies like Pfizer, Merck, Bristol Myers Squibb, and biotech firms regularly sponsor biostatisticians. They depend on specialized statistical expertise for drug development and FDA submissions, making them more willing to navigate visa processes than companies in other industries.
Can I get sponsored without prior U.S. clinical research experience?
Yes, but you'll need to demonstrate equivalent experience with regulatory frameworks like ICH-GCP or experience with similar agencies like EMA in Europe. Highlighting transferable skills in survival analysis, adaptive trial designs, and statistical programming languages strengthens your application significantly.
What is the prevailing wage requirement for sponsored Biostatistician 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.