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Senior Statistical Analyst - job 1 of 2

Company Description

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 – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on XFacebookInstagramYouTubeLinkedIn and Tik Tok.

Job Description

The Senior Statistical Analyst is a key role in the research and development of new pharmaceutical products. The primary responsibilities for this role include the analysis and reporting of clinical trial data and leading the statistical programming activities for clinical studies and projects with lower complexity. The Senior Statistical Analyst interfaces with Statistics, Data Sciences, Medical Writing, Regulatory Publishing and Clinical Operations.

  • Leads the statistical programming activities for projects with lower complexity.
  • Leads the statistical programming activities for studies.
  • Develop SAS programs for the creation of ADaM data sets following CDISC standards.
  • Develop SAS programs for the creation of Tables, Listings and Figures.
  • Validation of ADaM data sets, Tables, Listings and Figures.
  • Create specifications for the structure of ADaM data sets for individual studies and integrated data.
  • Create documentation for regulatory filings including reviewers guides and data definition documents
  • Leads the development of standard SAS Macros and participates in the development of standard operating procedures.
  • Provides oversight and mentoring of assigned Statistical Programmers and Statistical Analysts.

Qualifications

  • MS in Statistics, Computer Science or a related field with 6+ years of relevant experience. OR BS in Statistics, Computer Science or a related field with 8+ years of relevant experience.
  • Indepth understanding of SAS programming concepts and techniques related to drug development.
  • Fundamental understanding of CDISC Standards.
  • Fundamental understanding of the drug development process, including experience with regulatory filings.
  • Ability to communicate clearly both oral and written.
  • Ability to accurately estimate effort required for study related programming activities.

This a remote opportunity and can be hired anywhere in the US. 

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, serving our community and embracing diversity and inclusion.  It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.

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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What You Should Know About Senior Statistical Analyst, AbbVie

Join AbbVie as a Senior Statistical Analyst and be a crucial part of our mission to discover and deliver innovative medicines that improve lives. Based in Branchburg, NJ, this role is all about diving deep into the statistical analysis and reporting of clinical trial data. If you're someone who thrives in collaborative environments, you'll love working with teams across Statistics, Data Sciences, Medical Writing, and more! Your main duties will include leading statistical programming activities for clinical studies, developing SAS programs for creating ADaM datasets, and setting up Tables, Listings, and Figures that meet high industry standards. You'll also get the chance to mentor junior Statistical Programmers and provide oversight on key projects. To be a perfect fit, we’re looking for candidates with either a Master’s or Bachelor’s degree in Statistics or a related field, along with substantial experience in SAS programming and familiarity with CDISC standards. Enjoy the flexibility of a remote working opportunity while making a significant impact in the pharmaceutical realm. Apply today and help us tackle the medical challenges of tomorrow!

Frequently Asked Questions (FAQs) for Senior Statistical Analyst Role at AbbVie
What are the main responsibilities of a Senior Statistical Analyst at AbbVie?

As a Senior Statistical Analyst at AbbVie, you will lead the statistical programming activities for various clinical studies, analyze and report data from clinical trials, and develop SAS programs to create ADaM datasets, Tables, Listings, and Figures. You'll also be responsible for validating data outputs and creating necessary documentation for regulatory filings, all while mentoring and overseeing junior statistical personnel.

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What qualifications are required for the Senior Statistical Analyst position at AbbVie?

Candidates for the Senior Statistical Analyst role at AbbVie should hold a Master’s degree in Statistics, Computer Science, or a related field with at least 6 years of relevant experience, or a Bachelor’s degree with 8 years of experience. A strong understanding of SAS programming, CDISC standards, and the drug development process is essential for this position.

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Is the Senior Statistical Analyst position at AbbVie a remote work opportunity?

Yes! The Senior Statistical Analyst position at AbbVie is a remote opportunity, allowing you to work from anywhere in the U.S. This flexibility supports a great work-life balance while being part of a groundbreaking company in the pharmaceutical industry.

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What skills are vital for success as a Senior Statistical Analyst at AbbVie?

Key skills for success as a Senior Statistical Analyst at AbbVie include expertise in SAS programming, a solid understanding of statistical analysis methods, great communication abilities, and the capacity to work collaboratively across diverse scientific teams. Familiarity with regulatory processes and the ability to mentor others is also highly beneficial.

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What does the career growth look like for a Senior Statistical Analyst at AbbVie?

At AbbVie, a Senior Statistical Analyst has considerable opportunities for career growth. You can take on more complex projects, expand your leadership capabilities, and increase your involvement in strategic decision-making processes in clinical research and development, paving the way for potential advancement into senior management or specialized roles.

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Common Interview Questions for Senior Statistical Analyst
Can you explain your experience with SAS programming in relation to clinical trials?

In your response, highlight specific projects where you used SAS for data analysis, the types of datasets you created, and any challenges you overcame. Emphasize your understanding of statistical programming concepts and CDISC standards, showcasing your technical skills alongside your problem-solving abilities.

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How do you ensure the accuracy and consistency of clinical trial data?

Discuss your methodologies for data validation, quality checks, and any tools you use to maintain data integrity. Explaining processes such as peer review and cross-functional communication can illustrate your commitment to accuracy in clinical analysis.

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Describe a challenging project you led as a statistical analyst.

When answering, focus on the situation, the specific challenge you faced, the action you took to address it, and the outcome. This structure—often called the STAR method—demonstrates your analytical skills and your ability to manage difficult scenarios effectively.

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What is your understanding of CDISC standards and their importance?

It's important to demonstrate not only your knowledge of CDISC standards but also how they apply within the context of drug development and regulatory submissions. Discuss your experience in applying these standards in your previous roles and how you ensure compliance in your data management processes.

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How do you approach statistical programming tasks with lower complexity?

Discuss your strategies for breaking down projects, estimating time and resources needed, and the importance of clarity in specifications. Highlight examples where your organized approach helped streamline programming tasks and improve deliverables.

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How do you mentor junior analysts and statisticians?

Share your philosophy on mentorship, including how you provide guidance and support, facilitate learning opportunities, and foster an inclusive environment for questions and discussions. Mention specific instances where you helped a colleague improve their statistical skills or understanding.

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What experience do you have with regulatory filing documentation?

Outline your past experiences preparing documentation necessary for regulatory submissions. Explain your understanding of what information regulators look for and how you tailor documents to meet these requirements, emphasizing your attention to detail and compliance.

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Why do you want to work for AbbVie as a Senior Statistical Analyst?

Highlight your alignment with AbbVie’s mission and values, and discuss specific aspects of their innovative work that excite you. Your enthusiasm for the pharmaceutical industry and eagerness to contribute to meaningful health solutions can help illustrate your passion and commitment to the role.

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How do you stay updated with new statistical methods or technologies?

Talk about your continuous learning habits, such as attending workshops, participating in webinars, reading academic journals, or being involved in professional organizations. This shows your proactive approach and commitment to professional development.

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What project management skills do you possess that are relevant to this role?

Discuss your ability to plan, execute, and oversee projects from start to finish. Detail your experience with task prioritization, time management, and communicating with stakeholders, showcasing your capability in delivering projects effectively in a collaborative setting.

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AbbVie’s mission is to discover and deliver innovative medicines 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: i...

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DATE POSTED
March 13, 2025

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