Senior Researcher Jobs at AbbVie with Visa Sponsorship
AbbVie hires Senior Researchers across 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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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.
Job Description
The Safety Statistics Group (SSG) at AbbVie is an important strategic part of Data and Statistical Sciences (DSS). Safety Statisticians are part of collaborative, cross functional teams including members from Pharmacovigilance and Patient Safety (e.g, product safety team physicians, epidemiologists, safety analysts), Statistical Programming, Clinical Statistics, Regulatory Affairs, and Medical Writing. Safety Statisticians work on products in the AbbVie portfolio ranging from early to later stages of development and life cycle management, with a focus on evaluation, interpretation, and reporting of aggregate/integrated safety data, including benefit risk planning and assessment. AbbVie is seeking a statistician to join our growing Safety Statistics team. The Senior Research Statistician in the Safety Statistics Group will work collaboratively with senior-level statisticians in supporting one or more Product Safety Teams (PSTs).
Key Responsibilities:
- Contribute to the development of Product Safety Statistical Analysis Plans and Integrated Summary of Safety Statistical Analysis Plans.
- Contribute to the development of safety data integration specifications in accordance with analysis plan.
- Contribute to benefit-risk planning and assessment.
- Contribute to the development, delivery and interpretation of safety outputs, including graphics.
- Contribute to cross-functional development of output specifications to address both pre-planned safety analyses and ad hoc requests.
- Collaborate with Statistical Programming to ensure the delivery of high-quality outputs according to agreed-upon timelines.
- Ensure appropriate interpretation of safety deliverables in collaboration with other functions.
- Collaborate within SSG 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.
- Stay current with industry trends and practices related to safety.
Qualifications
Minimum Qualifications:
- MS (with at least 4 years of relevant experience) or PhD in Statistics, Biostatistics, or a highly related field
- Experience in clinical trial setting and doing submissions
- Experience with safety data
- SAS Programming Experience
- High degree of competence in experimental design, descriptive and inferential statistics, and statistical programming
Preferred Qualifications:
- Simulation experience
- Experience programming in R
- R Shiny Experience
Key Leadership Competencies:
- Builds strong relationships with peers and cross functionality with partners outside of team to enable higher performance
- Learns fast, grasps the ‘essence’ and can change the course quickly where indicated
- Raises the bar and is never satisfied with the status quo
- Creates a learning environment, open to suggestions and experimentation for improvement
- Embraces the ideas of others, nurtures and manages innovation to reality
- Good oral and written English communication skills
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.
Job Description
The Safety Statistics Group (SSG) at AbbVie is an important strategic part of Data and Statistical Sciences (DSS). Safety Statisticians are part of collaborative, cross functional teams including members from Pharmacovigilance and Patient Safety (e.g, product safety team physicians, epidemiologists, safety analysts), Statistical Programming, Clinical Statistics, Regulatory Affairs, and Medical Writing. Safety Statisticians work on products in the AbbVie portfolio ranging from early to later stages of development and life cycle management, with a focus on evaluation, interpretation, and reporting of aggregate/integrated safety data, including benefit risk planning and assessment. AbbVie is seeking a statistician to join our growing Safety Statistics team. The Senior Research Statistician in the Safety Statistics Group will work collaboratively with senior-level statisticians in supporting one or more Product Safety Teams (PSTs).
Key Responsibilities:
- Contribute to the development of Product Safety Statistical Analysis Plans and Integrated Summary of Safety Statistical Analysis Plans.
- Contribute to the development of safety data integration specifications in accordance with analysis plan.
- Contribute to benefit-risk planning and assessment.
- Contribute to the development, delivery and interpretation of safety outputs, including graphics.
- Contribute to cross-functional development of output specifications to address both pre-planned safety analyses and ad hoc requests.
- Collaborate with Statistical Programming to ensure the delivery of high-quality outputs according to agreed-upon timelines.
- Ensure appropriate interpretation of safety deliverables in collaboration with other functions.
- Collaborate within SSG 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.
- Stay current with industry trends and practices related to safety.
Qualifications
Minimum Qualifications:
- MS (with at least 4 years of relevant experience) or PhD in Statistics, Biostatistics, or a highly related field
- Experience in clinical trial setting and doing submissions
- Experience with safety data
- SAS Programming Experience
- High degree of competence in experimental design, descriptive and inferential statistics, and statistical programming
Preferred Qualifications:
- Simulation experience
- Experience programming in R
- R Shiny Experience
Key Leadership Competencies:
- Builds strong relationships with peers and cross functionality with partners outside of team to enable higher performance
- Learns fast, grasps the ‘essence’ and can change the course quickly where indicated
- Raises the bar and is never satisfied with the status quo
- Creates a learning environment, open to suggestions and experimentation for improvement
- Embraces the ideas of others, nurtures and manages innovation to reality
- Good oral and written English communication skills
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
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Get Access To All JobsTips for Finding Senior Researcher Jobs at AbbVie Jobs
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.
Senior Researcher at AbbVie jobs are hiring across the US. Find yours.
Find Senior Researcher at AbbVie JobsFrequently 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 (for Australian citizens), H-1B1 (for Chilean and Singaporean nationals), TN (for Canadian and Mexican professionals), F-1 OPT and CPT, J-1 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.
See which Senior Researcher at AbbVie employers are hiring and sponsoring visas right now.
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