Senior Researcher Jobs at AbbVie with Visa Sponsorship
Senior Researcher jobs at AbbVie span therapeutic areas including oncology, immunology, and neuroscience, with roles typically requiring advanced degrees and specialized lab or translational research experience. AbbVie has an established sponsorship infrastructure that supports international researchers across multiple visa categories throughout the employment lifecycle.
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Get Access To All JobsCompany Description
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
Job Description
The Senior Research Statistician, Statistics is responsible for providing statistical support to the research and development organization. Specific areas of work may include clinical trials, patient safety, and global medical affairs (GMA). The Senior Research Statistician works in partnership with experts in multiple disciplines to advance medicines to our patients.
Major Job Responsibilities
-
Contribute to design, analysis and reporting of clinical trials or other scientific research studies. Assist with development of protocols and/or statistical analysis plans (or product safety analysis plans/integrated summary of safety analysis plans/analysis plans for GMA evidence generation) with details for programming implementation. Work under supervision to implement sound statistical methodology in scientific investigations.
-
Assist in identifying scientifically appropriate data collection instruments. Identify and report data issues or violations of study assumptions. Provide programming specifications for derived variables and analysis datasets. Collaborate with Data Science in preparing for database lock.
-
With supervision perform statistical analyses as per the analysis plan. Collaborate with Statistical Programming to ensure the delivery of high-quality outputs according to agreed-upon timelines. Evaluate appropriateness of available software for planned analyses and assess needs for potential development of novel statistical methodology.
-
With supervision, develop strategy for data presentation and inference. Ensure appropriate interpretation of statistical deliverables in collaboration with other functions. Collaborate in publication of scientific research. Ensure accuracy and internal consistency of reports and publications, including tables, listings, and figures. Ensure the accuracy of the statistical component of scientific reports and/or publications with high quality.
-
Work collaboratively with cross-functional teams. Clearly explain statistical concepts to non-statisticians. Provide responses to questions and pursue analyses suggested by data under supervision. Support communications between assigned product team(s) and functional management. Build/drive cross-functional relationships and collaboration.
-
(SSG) Contribute to benefit-risk planning and assessment. Contribute to cross-functional development of output specifications to address both pre-planned safety analyses and ad hoc requests.
-
(SSG) Collaborate within the Safety Statistics Group to implement strategic initiatives that address processes related to interpreting, monitoring, assessing, and reporting safety data to better characterize the safety profile of AbbVie products, improve efficiencies, and provide greater consistency across therapeutic areas.
-
(GMA Stat) In collaboration with GMA, Clinical Statistics, Data Sciences, Statistical Programming and other stakeholders to evaluate existing databases, both clinical studies and real-world databases, assist with feasibility assessment to identify fit-for-purpose data sources to address research questions, and develop detailed and actionable analysis plans for evidence generation to deliver high quality, patient-centric evidence and insights to drive decisions.
Qualifications
Minimum Qualifications:
- MS or PhD in Statistics, Biostatistics, or a highly related field.
- 4+ years of experience performing statistical computations and simulations.
Preferred Qualifications:
- Experience in oncology.
Other Required Skills:
- High degree of technical competence and effective communication skills, both oral and written.
- Able to build strong relationships with peers and cross-functional partners to achieve higher performance.
- Highly motivated to drive innovation by raising the bar and challenging the status quo.
- Able to identify data or analytical issues, and assist with providing solutions by either applying own skills and knowledge or seeking help from others.
Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
-
The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
-
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
-
This job is eligible to participate in our short-term incentive programs.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html
Company Description
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
Job Description
The Senior Research Statistician, Statistics is responsible for providing statistical support to the research and development organization. Specific areas of work may include clinical trials, patient safety, and global medical affairs (GMA). The Senior Research Statistician works in partnership with experts in multiple disciplines to advance medicines to our patients.
Major Job Responsibilities
-
Contribute to design, analysis and reporting of clinical trials or other scientific research studies. Assist with development of protocols and/or statistical analysis plans (or product safety analysis plans/integrated summary of safety analysis plans/analysis plans for GMA evidence generation) with details for programming implementation. Work under supervision to implement sound statistical methodology in scientific investigations.
-
Assist in identifying scientifically appropriate data collection instruments. Identify and report data issues or violations of study assumptions. Provide programming specifications for derived variables and analysis datasets. Collaborate with Data Science in preparing for database lock.
-
With supervision perform statistical analyses as per the analysis plan. Collaborate with Statistical Programming to ensure the delivery of high-quality outputs according to agreed-upon timelines. Evaluate appropriateness of available software for planned analyses and assess needs for potential development of novel statistical methodology.
-
With supervision, develop strategy for data presentation and inference. Ensure appropriate interpretation of statistical deliverables in collaboration with other functions. Collaborate in publication of scientific research. Ensure accuracy and internal consistency of reports and publications, including tables, listings, and figures. Ensure the accuracy of the statistical component of scientific reports and/or publications with high quality.
-
Work collaboratively with cross-functional teams. Clearly explain statistical concepts to non-statisticians. Provide responses to questions and pursue analyses suggested by data under supervision. Support communications between assigned product team(s) and functional management. Build/drive cross-functional relationships and collaboration.
-
(SSG) Contribute to benefit-risk planning and assessment. Contribute to cross-functional development of output specifications to address both pre-planned safety analyses and ad hoc requests.
-
(SSG) Collaborate within the Safety Statistics Group to implement strategic initiatives that address processes related to interpreting, monitoring, assessing, and reporting safety data to better characterize the safety profile of AbbVie products, improve efficiencies, and provide greater consistency across therapeutic areas.
-
(GMA Stat) In collaboration with GMA, Clinical Statistics, Data Sciences, Statistical Programming and other stakeholders to evaluate existing databases, both clinical studies and real-world databases, assist with feasibility assessment to identify fit-for-purpose data sources to address research questions, and develop detailed and actionable analysis plans for evidence generation to deliver high quality, patient-centric evidence and insights to drive decisions.
Qualifications
Minimum Qualifications:
- MS or PhD in Statistics, Biostatistics, or a highly related field.
- 4+ years of experience performing statistical computations and simulations.
Preferred Qualifications:
- Experience in oncology.
Other Required Skills:
- High degree of technical competence and effective communication skills, both oral and written.
- Able to build strong relationships with peers and cross-functional partners to achieve higher performance.
- Highly motivated to drive innovation by raising the bar and challenging the status quo.
- Able to identify data or analytical issues, and assist with providing solutions by either applying own skills and knowledge or seeking help from others.
Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
-
The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
-
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
-
This job is eligible to participate in our short-term incentive programs.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html
See all Senior Researcher Jobs at AbbVie
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Senior Researcher Jobs at AbbVie.
Get Access To All JobsTips for Finding Senior Researcher Jobs at AbbVie
Align your research specialty with AbbVie's pipeline
AbbVie's Senior Researcher openings cluster around its core therapeutic areas: oncology, immunology, and neuroscience. Reviewing its pipeline on its investor relations page before applying lets you frame your CV around the disease areas where active headcount is growing.
Verify your degree meets specialty occupation standards
USCIS requires a directly related bachelor's degree or higher for H-1B classification. For a Senior Researcher role, a PhD in a relevant biological or chemical science field strengthens the petition significantly, since AbbVie's job requirements typically specify advanced degrees for this level.
Target AbbVie's North Chicago and Bay Area sites
AbbVie's Senior Researcher postings concentrate at its North Chicago headquarters and California research sites. Filtering your job search by these locations surfaces the highest-activity hiring clusters and connects you with the research divisions that sponsor the most international candidates.
Use Migrate Mate to find open Senior Researcher roles at AbbVie
Sponsorship-eligible Senior Researcher positions at AbbVie are not always clearly labeled on general job boards. Use Migrate Mate to filter AbbVie postings by visa type so you're applying only to roles where international candidates are actively considered.
Prepare for AbbVie's LCA public access file requirements
Before AbbVie files your H-1B petition, it must submit a Labor Condition Application to the DOL certifying your offered wage meets the prevailing wage for your work location. Request the LCA details from your recruiting contact so you can verify the position and worksite are correctly documented.
Negotiate start dates around H-1B cap timelines
If you're applying outside AbbVie's cap-exempt affiliates and need a new H-1B, USCIS cap filings open in April for an October 1 start. Build this into your offer negotiation early so your start date is realistic and the offer letter reflects the correct employment commencement window.
Frequently Asked Questions
Does AbbVie sponsor H-1B visas for Senior Researchers?
Yes, AbbVie sponsors H-1B visas for Senior Researcher roles. The company has an established immigration infrastructure and works with immigration counsel to file H-1B petitions for qualifying candidates. Senior Researcher positions typically satisfy USCIS specialty occupation requirements given the advanced degree and discipline-specific expertise the roles demand.
How do I apply for Senior Researcher jobs at AbbVie?
Applications go through AbbVie's careers portal at abbvie.com/careers. Search by job function (Research and Development) and filter by location to find active Senior Researcher openings. You can also browse sponsorship-eligible postings directly on Migrate Mate, which surfaces roles where AbbVie is actively considering international candidates, saving you time filtering through listings that don't apply to your situation.
Which visa types does AbbVie commonly use for Senior Researcher roles?
AbbVie sponsors a range of visa categories for Senior Researchers, including H-1B, E-3 visa (for Australian citizens), H-1B1 visa (for Chilean and Singaporean nationals), TN visa (for Canadian and Mexican professionals), F-1 OPT and CPT, J-1 visa research scholars, and employment-based Green Card pathways through EB-2 and EB-3. The right category depends on your nationality, degree, and career stage.
What qualifications does AbbVie expect for Senior Researcher positions?
AbbVie typically requires a PhD in a relevant life science discipline such as biology, biochemistry, pharmacology, or chemistry for Senior Researcher roles, often with postdoctoral or industry research experience. Proficiency in specific methodologies, such as CRISPR, high-throughput screening, or translational biomarker work, frequently appears in job descriptions aligned with AbbVie's therapeutic pipeline.
How do I plan my timeline if I need H-1B sponsorship from AbbVie?
If you need a new cap-subject H-1B, USCIS accepts petitions starting in April each year for an October 1 start date. You'll want an offer finalized before March to give AbbVie's legal team adequate preparation time. F-1 students on OPT can often start earlier if their OPT is still valid, with AbbVie filing the H-1B to extend authorization ahead of the expiration.