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AbbVie - North Chicago, IL

posted 3 months ago

Full-time - Mid Level
North Chicago, IL
Chemical Manufacturing

About the position

The Senior Manager, Statistics role at AbbVie is focused on ensuring the integrity and quality of statistical methodologies applied in clinical trials and research projects. This position involves collaborating with project teams to design studies, select appropriate statistical methods, and ensure the accuracy of data analysis and reporting. The role requires a deep understanding of statistical concepts and the ability to communicate complex results effectively to various stakeholders.

Responsibilities

  • Ensure consistency among protocols within a project and certify the protocol review checklist.
  • Select appropriate study designs to meet study objectives and contribute to data collection instrument decisions.
  • Conduct comprehensive reviews of protocols to ensure quality and identify key parameters for sample size estimation.
  • Determine appropriate statistical methodologies to support study objectives and author the statistical methods section of protocols.
  • Manage randomization for routine and non-routine studies and collaborate with external partners for implementation.
  • Participate in meetings to identify data collection instruments and database design requirements to ensure data quality.
  • Evaluate alternative statistical approaches and make recommendations based on sound statistical reasoning.
  • Develop strategies for data presentation and ensure consistency in scientific arguments across project deliverables.
  • Prepare oral and written reports communicating research results to various stakeholders.
  • Collaborate with multi-functional teams to complete project deliverables on time and keep management informed of important issues.
  • Represent Data and Statistical Sciences on project teams to provide functional input and ensure alignment of priorities.
  • Maintain technical skills and knowledge of new statistical methodologies through literature and professional meetings.

Requirements

  • MS or PhD in Statistics, Biostatistics, or a highly related field.
  • 4-6 years of experience in pharmaceutical development and applied statistics (PhD) or 8-10 years (MS).
  • Experience with statistical modeling and inferential statistics.
  • Knowledge of new/novel statistical techniques and their applications in biopharmaceuticals.
  • Experience in the pharmaceutical industry with nonclinical, clinical, or pharmacology studies.

Nice-to-haves

  • Experience in a regulated environment related to drug development.
  • Understanding of drug development processes.

Benefits

  • Health insurance
  • 401k plan
  • Paid holidays
  • Flexible scheduling
  • Professional development opportunities
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