TN Visa Analytics Manager Jobs
Analytics Manager roles qualify for TN visa sponsorship under the USMCA treaty's Management Consultant or Statistician categories, depending on your responsibilities and degree. Canadian professionals can apply at the port of entry; Mexican citizens use consular processing. A bachelor's degree in a quantitative field and a qualifying job offer are required.
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Get Access To All JobsINTRODUCTION
Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based immunotherapy. From our three R&D sites around the world, we apply these innovative technologies to pursue the discovery of safe, efficacious and cutting-edge therapeutics for patients worldwide.
Legend Biotech entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop and commercialize ciltacabtagene autolecuel (cilta-cel). Our strategic partnership is designed to combine the strengths and expertise of both companies to advance the promise of an immunotherapy in the treatment of multiple myeloma.
Legend Biotech is seeking a Sr. Manager, Biostatistician/Programmer as part of the Clinical team based in Somerset, NJ.
ROLE OVERVIEW
The Sr. Manager, Biostatistician/Programmer plays a critical hands-on role in supporting Legend Biotech's clinical development programs by transforming clinical trial data into high-quality analyses, tables, figures, and listings that inform decision-making. This role partners closely with clinical, translational, research stakeholders to deliver timely insights, conduct exploratory and ad hoc analyses, and deeply understand the medical and scientific questions underlying the data. The position requires strong programming expertise, data agility, intellectual curiosity, and the ability to work independently in a fast-moving biotech environment.
KEY RESPONSIBILITIES
- Develop, validate, and maintain high-quality Tables, Figures, and Listings (TFLs) to support ongoing clinical trials, interim analyses, and internal/external deliverables in compliance with study requirements and standards.
- Perform hands-on statistical programming and data manipulation to support planned and ad hoc analyses, addressing evolving clinical and scientific questions.
- Independently explore and interrogate clinical trial data to identify trends, anomalies, and insights that support clinical interpretation and decision-making.
- Collaborate closely with Biostatistics, Clinical Development, Clinical Operations, Data Management, Translational research and Medical teams to ensure alignment of analyses with protocol objectives and clinical intent.
- Apply a strong understanding of therapeutic area, disease biology, and clinical endpoints to translate data into meaningful scientific insights.
- Contribute to analysis datasets, program specifications, programming documentation, and quality control activities in accordance with internal standards and regulatory expectations.
- Support process improvement initiatives, including enhancing programming efficiency, standardization, and reproducibility across studies and programs.
- This role operates with a high degree of autonomy in determining programming approaches, exploratory analyses, and data interrogation strategies to answer clinical questions. The Sr. Manager may independently make decisions related to analysis methods, programming solutions, prioritization of tasks, and investigative follow-up of data issues. Escalation and alignment are expected for changes impacting study-level strategy, major deliverables, timelines with external visibility, or regulatory-facing outputs.
REQUIREMENTS
- Master's degree or PhD in Statistics, Biostatistics, Mathematics, Data Science, or a related quantitative discipline.
- Demonstrated hands-on experience developing TFLs and performing ad hoc and exploratory analyses for clinical trials.
- Strong understanding of clinical trial design, clinical data structures, and the medical context behind analyses.
- Proven ability to work independently, manage ambiguity, and drive self-directed discovery from data.
- Experience supporting oncology and/or cell therapy programs is strongly preferred.
- Advanced proficiency in SAS for clinical trial analysis and reporting.
- Working knowledge of R for exploratory analyses and data visualization.
- Strong experience with clinical data standards (e.g., SDTM, ADaM).
- Experience with or strong willingness to leverage AI-assisted programming tools to accelerate development, enhance code quality, and support efficient generation of Tables, Figures, and Listings (TFLs).
Li-JR1
Li-Hybrid
Please note: These benefits are offered exclusively to permanent full-time employees. Contractors are not eligible for benefits through Legend Biotech.
EEO STATEMENT
It is the policy of Legend Biotech to provide equal employment opportunities without regard to actual or perceived race, color, creed, religion, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth, related medical conditions and lactation), gender identity or gender expression (including transgender status), sexual orientation, marital status, military service and veteran status, disability, genetic information, or any other protected characteristic under applicable federal, state or local laws or ordinances.
Employment is at-will and may be terminated at any time with or without cause or notice by the employee or the company.
For information related to our privacy notice, please review: Legend Biotech Privacy Notice.
INTRODUCTION
Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based immunotherapy. From our three R&D sites around the world, we apply these innovative technologies to pursue the discovery of safe, efficacious and cutting-edge therapeutics for patients worldwide.
Legend Biotech entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop and commercialize ciltacabtagene autolecuel (cilta-cel). Our strategic partnership is designed to combine the strengths and expertise of both companies to advance the promise of an immunotherapy in the treatment of multiple myeloma.
Legend Biotech is seeking a Sr. Manager, Biostatistician/Programmer as part of the Clinical team based in Somerset, NJ.
ROLE OVERVIEW
The Sr. Manager, Biostatistician/Programmer plays a critical hands-on role in supporting Legend Biotech's clinical development programs by transforming clinical trial data into high-quality analyses, tables, figures, and listings that inform decision-making. This role partners closely with clinical, translational, research stakeholders to deliver timely insights, conduct exploratory and ad hoc analyses, and deeply understand the medical and scientific questions underlying the data. The position requires strong programming expertise, data agility, intellectual curiosity, and the ability to work independently in a fast-moving biotech environment.
KEY RESPONSIBILITIES
- Develop, validate, and maintain high-quality Tables, Figures, and Listings (TFLs) to support ongoing clinical trials, interim analyses, and internal/external deliverables in compliance with study requirements and standards.
- Perform hands-on statistical programming and data manipulation to support planned and ad hoc analyses, addressing evolving clinical and scientific questions.
- Independently explore and interrogate clinical trial data to identify trends, anomalies, and insights that support clinical interpretation and decision-making.
- Collaborate closely with Biostatistics, Clinical Development, Clinical Operations, Data Management, Translational research and Medical teams to ensure alignment of analyses with protocol objectives and clinical intent.
- Apply a strong understanding of therapeutic area, disease biology, and clinical endpoints to translate data into meaningful scientific insights.
- Contribute to analysis datasets, program specifications, programming documentation, and quality control activities in accordance with internal standards and regulatory expectations.
- Support process improvement initiatives, including enhancing programming efficiency, standardization, and reproducibility across studies and programs.
- This role operates with a high degree of autonomy in determining programming approaches, exploratory analyses, and data interrogation strategies to answer clinical questions. The Sr. Manager may independently make decisions related to analysis methods, programming solutions, prioritization of tasks, and investigative follow-up of data issues. Escalation and alignment are expected for changes impacting study-level strategy, major deliverables, timelines with external visibility, or regulatory-facing outputs.
REQUIREMENTS
- Master's degree or PhD in Statistics, Biostatistics, Mathematics, Data Science, or a related quantitative discipline.
- Demonstrated hands-on experience developing TFLs and performing ad hoc and exploratory analyses for clinical trials.
- Strong understanding of clinical trial design, clinical data structures, and the medical context behind analyses.
- Proven ability to work independently, manage ambiguity, and drive self-directed discovery from data.
- Experience supporting oncology and/or cell therapy programs is strongly preferred.
- Advanced proficiency in SAS for clinical trial analysis and reporting.
- Working knowledge of R for exploratory analyses and data visualization.
- Strong experience with clinical data standards (e.g., SDTM, ADaM).
- Experience with or strong willingness to leverage AI-assisted programming tools to accelerate development, enhance code quality, and support efficient generation of Tables, Figures, and Listings (TFLs).
Li-JR1
Li-Hybrid
Please note: These benefits are offered exclusively to permanent full-time employees. Contractors are not eligible for benefits through Legend Biotech.
EEO STATEMENT
It is the policy of Legend Biotech to provide equal employment opportunities without regard to actual or perceived race, color, creed, religion, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth, related medical conditions and lactation), gender identity or gender expression (including transgender status), sexual orientation, marital status, military service and veteran status, disability, genetic information, or any other protected characteristic under applicable federal, state or local laws or ordinances.
Employment is at-will and may be terminated at any time with or without cause or notice by the employee or the company.
For information related to our privacy notice, please review: Legend Biotech Privacy Notice.
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Get Access To All JobsTips for Finding TN Visa Sponsorship as an Analytics Manager
Align your degree to the right TN category
Analytics Manager roles can qualify under Management Consultant or Statistician depending on your duties. Your degree field must match the category you claim, so confirm the alignment before applying rather than after receiving an offer.
Build a role-specific support letter with your employer
CBP officers assess whether your Analytics Manager duties genuinely fit a qualifying TN visa occupation. Ask your employer to describe your data modeling, statistical analysis, or strategy functions explicitly, not just your job title.
Target employers with established data analytics teams
Companies running dedicated analytics functions, not just IT departments, are more comfortable with TN sponsorship paperwork. Look for postings that mention SQL, Python, or machine learning rather than general business analysis or reporting.
Prepare your Canadian or Mexican credentials documentation early
Your degree transcripts and any professional certifications must demonstrate a direct connection to your analytical role. If your degree title is broad, a credential evaluation or employer letter clarifying the technical focus strengthens your TN package.
Use Migrate Mate to find employers already open to TN sponsorship
Not every employer advertising Analytics Manager roles will sponsor a TN visa. Migrate Mate filters opportunities by TN sponsorship readiness, so you apply to companies already prepared to support your status rather than discovering gaps after an offer.
Prepare for secondary inspection if your duties span multiple categories
If your Analytics Manager role blends consulting, statistical modeling, and systems work, CBP may ask clarifying questions at the port of entry. Carrying a clear duty breakdown document prepared by your employer reduces the risk of a delay.
Analytics Manager TN Visa: Frequently Asked Questions
Does an Analytics Manager role qualify for a TN visa?
Yes, but the qualifying category depends on your actual duties. If your role focuses on statistical modeling and data interpretation, Statistician is the stronger fit. If it centers on advising business units on data strategy, Management Consultant applies. Your job offer letter and support documentation must reflect whichever category you claim, and your degree must align with it.
How does the TN visa compare to H-1B for Analytics Manager positions?
The TN visa has no annual lottery and no cap for Canadian citizens, so you can start work as soon as CBP approves your application at the port of entry. H-1B visa requires winning a lottery with roughly a one-in-four chance and waiting up to a year to begin work. For Mexican citizens, TN has a cap of 5,500 per year but still avoids the lottery. Analytics Managers who qualify for TN face significantly less uncertainty in their timeline.
Can I switch Analytics Manager jobs while on a TN visa?
Yes, but your TN status is tied to your approved employer and role. Before your last day with your current employer, you need a new TN approval based on an offer from the incoming company. Canadians can get this approved at the border; Mexican citizens must schedule a consular appointment. Gaps in employment status are the most common complication, so timing matters.
How do I find Analytics Manager jobs where the employer will sponsor a TN visa?
Many job postings don't specify TN sponsorship willingness, which makes identifying the right employers time-consuming. Migrate Mate is built specifically for this, filtering Analytics Manager opportunities by TN visa sponsorship so you're not spending weeks on outreach to employers who can't or won't support your status. Focusing your search there shortens the process considerably.
What documents does my employer need to provide for my TN application as an Analytics Manager?
Your employer must provide a support letter on company letterhead that describes your job title, your specific duties, your qualifications, the duration of employment, and confirmation that the role qualifies under a TN occupation category. For Analytics Managers, the letter should explicitly reference data analysis, statistical functions, or consulting responsibilities rather than generic management language, since CBP uses this document to verify category eligibility.