Manager, Statistics

Allergan

Chicago, Northern (IL, KY)

Hybrid

USD 120,000 - 180,000

Full time

4 days ago
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Job summary

AbbVie in Chicago, IL seeks a Manager, Statistics to provide statistical expertise to R&D, including design/analysis of clinical trials, patient safety, and global medical affairs.

The role collaborates with cross-functional teams to develop analysis plans, ensure data quality, and present results; requires MS or PhD in Statistics/Biostatistics with strong programming in SAS, R, or Python. Immunology trial experience preferred.

Qualifications

  • MS (with 6+ years of experience) or PhD (with 2+ years of experience) in Statistics, Biostatistics, or a highly related field.
  • Proficiency in SAS, R, and/or Python, with demonstrated expertise in developing, validating, and implementing complex statistical analyses and simulation studies.
  • Experience supporting clinical development programs, including clinical trial design and statistical analysis planning.
  • Ability to independently lead statistical activities for one or more studies and effectively communicate statistical concepts and results to cross-functional stakeholders.
  • Experience in the pharmaceutical, biotechnology, or healthcare industry.

Responsibilities

  • Provide expertise to design, analysis and reporting of clinical trials or other scientific research studies.
  • Independently develop protocols and/or statistical analysis plans with details for programming implementation.
  • Collaborate with Statistical Programming to ensure the delivery of high-quality outputs.
  • Develop strategy for data presentation and inference; collaborate in publication of scientific research.
  • Work collaboratively with multifunction teams; explain statistical concepts to non-statisticians.

Skills

SAS
R
Python
Statistical analyses

Education

MS in Statistics/ Biostatistics
PhD in Statistics/Biostatistics

Tools

SAS

Job description

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 Manager, Statistics provides statistical expertise to support the research and development organization. Specific areas of work may include clinical trials, patient safety, and global medical affairs. The Manager works independently in partnership with experts in multiple disciplines to advance medicines to our patients.

Responsibilities
  • Provide expertise to design, analysis and reporting of clinical trials or other scientific research studies. Independently develop 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. Implement sound statistical methodology in scientific investigations.
  • Identify scientifically appropriate data collection instruments. Identify and report data issues or violations of study assumptions. Provide programming specifications for derived variables and analysis datasets. Partner with Data Science in preparing for database lock.
  • Independently 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. Identify and anticipate issues arising in the study design, conduct and propose scientifically sound approaches. Evaluate appropriateness of available software for planned analyses and assess needs for potential development of novel statistical methodology.
  • Develop strategy for data presentation and inference. Collaborate in publication of scientific research. Ensure accuracy and internal consistency of reports and publications, including tables, listings, and figures. Ensure that study results and conclusions are scientifically sound, clearly presented, and consistent with statistical analyses provided.
  • Work collaboratively with multifunction teams. Clearly explain statistical concepts to non-statisticians. Provide responses to questions, and pursue analyses suggested by data. Support communications between assigned product team(s) and functional management. Build/drive cross-functional relationships and collaboration.
  • (SSG) Collaborate with cross functional team for 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/lead within the Safety Statistics Group to implement strategic initiatives that address processes related to interpreting, monitoring, assessing, and reporting safety data to characterize the safety profile of AbbVie products, improve efficiencies, and provide 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, conduct 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 (with 6+ years of experience) or PhD (with 2+ years of experience) in Statistics, Biostatistics, or a highly related field.
  • Proficiency in SAS, R, and/or Python, with demonstrated expertise in developing, validating, and implementing complex statistical analyses and simulation studies.
  • Experience supporting clinical development programs, including clinical trial design and statistical analysis planning.
  • Ability to independently lead statistical activities for one or more studies and effectively communicate statistical concepts and results to cross-functional stakeholders.
  • Experience in the pharmaceutical, biotechnology, or healthcare industry.
Preferred Qualifications:
  • Immunology clinical trial experience
  • PhD in statistics, biostatistics or a highly related field
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 Companybelieves ingood faith it will pay for this role at the timeof this posting based on the job grade for this position.Individualcompensation paid within this range will depend on many factors including geographic location, andwemayultimatelypaymore or less than the posted range. This range may bemodifiedin thefuture.
  • We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),medical/dental/visioninsurance and 401(k) to eligibleemployees.
  • This job is eligible toparticipatein our long-term incentiveprograms.

Note: No amount of payis considered to bewages or compensation until such amount is earned, vested, anddeterminable.The amount and availability of any bonus,commission, incentive, benefits, or any other form ofcompensation and benefitsthat are allocable to a particular employeeremainsin the Company's sole andabsolutediscretion unless and until paid andmay bemodifiedat the Company’s sole and absolute discretion, consistent withapplicable 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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