Senior Statistician

Becton Dickinson

Franklin Lakes (NJ)

On-site

USD 90,000 - 130,000

Full time

4 days ago
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Job summary

BD is seeking a Statistician/Biostatistician to support product development, clinical studies, and regulatory decisions in a medical device environment. You will partner with cross-functional teams to design studies, develop analysis plans, and deliver actionable insights.

The role requires strong programming in R or SAS, experience in regulated healthcare settings, and the ability to communicate results through reports and presentations.

Qualifications

  • Master's degree in Statistics, Biostatistics, or related quantitative field.
  • 3+ years of experience in regulated healthcare, life sciences, or medical device environment.
  • Experience applying statistical methods to product development, clinical research, and/or clinical trials.
  • Proficiency in programming, documenting, and validating analyses using R and/or SAS.
  • Experience independently solving statistical and analytical challenges.
  • Experience leading and influencing cross-functional teams without direct authority.
  • Experience managing multiple projects and priorities in a fast-paced environment.
  • Experience in stakeholder management.

Responsibilities

  • Design, plan, analyze, and interpret studies and experiments supporting product development and business decisions.
  • Develop and review study protocols, CRFs, and regulatory documentation.
  • Develop and maintain statistical analysis plans; consult for complex situations.
  • Program, document, validate, and maintain statistical code in R and SAS.
  • Apply appropriate statistical methodologies to analytical challenges.
  • Prepare statistical reports and documentation for internal and external audiences.
  • Deliver high-quality analyses and insights across products and functions.
  • Stay current with emerging statistical methodologies and regulatory requirements.
  • Present statistical findings to stakeholders and contribute to publications.

Skills

Statistical analysis
Cross-functional collaboration
Project management
Communication
Stakeholder management
Problem solving

Education

Master's degree in Statistics/Biostatistics
PhD in Statistics/Biostatistics (preferred)

Tools

R
SAS

Job description

We are the people who give possibilities purpose

BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities.

Job Description

We are seeking a Statistician/Biostatistician to support product development, clinical studies, and business decision-making within a regulated healthcare or medical device environment. This role partners closely with cross-functional teams to design studies, develop statistical analysis plans, analyze complex data sets, and communicate actionable insights. The successful Statistician will apply advanced statistical methodologies, program and validate analyses in R or SAS, prepare technical reports, and help ensure projects meet quality, regulatory, and business objectives.

Key Responsibilities:
  • Partner with Medical Affairs and cross-functional project teams to design, plan, analyze, and interpret studies and experiments that support product development and business decision-making.
  • Contribute to the development and review of study protocols, case report forms, and other clinical and regulatory documentation.
  • Independently develop and maintain statistical analysis plans, seeking consultation for complex or non-routine situations as needed.
  • Program, document, validate, and maintain statistical code in R and/or SAS for data management, analysis, visualization, and reporting.
  • Apply appropriate statistical methodologies to address standard and complex analytical challenges.
  • Prepare clear, concise, and scientifically rigorous statistical reports and technical documentation for internal and external audiences.
  • Deliver high-quality statistical analyses and insights that support project milestones across multiple products, platforms, and business functions.
  • Stay current with emerging statistical methodologies, industry best practices, and evolving regulatory requirements.
  • Present statistical findings to cross-functional stakeholders and contribute to scientific publications, conference presentations, and external communications as appropriate.
Minimum Required:
  • Master's degree in Statistics, Biostatistics, or a related quantitative field (or equivalent combination of education and experience).
  • 3+ years of experience with a Master's degree, in regulated healthcare, life sciences, or medical device environment.
  • Demonstrated experience applying statistical methods to product development, clinical research, and/or clinical trials.
  • Proficiency in programming, documenting, and validating statistical analyses using R and/or SAS.
  • Experience independently solving statistical and analytical challenges.
  • Experience leading and influencing cross-functional teams without direct authority.
  • Experience managing multiple projects and priorities simultaneously in a fast-paced environment.
  • Experience with technical report writing and presentation of statistical findings.
  • Experience in stakeholder management.
Preferred Experience and Skills
  • PhD in Statistics, Biostatistics, or related quantitative discipline.
  • 1+ years of professional experience with a PhD
  • Experience applying statistical methodologies in manufacturing, quality, regulatory, process improvement, or operational excellence initiatives.
  • Knowledge of and experience working in a reproducible research environment.
  • Working knowledge of applicable healthcare, clinical, and medical device regulations, with the ability to independently apply regulatory requirements.
  • Experience supporting submissions, regulatory interactions, or compliance-related statistical activities.
  • Publication or presentation experience at scientific conferences, industry forums, or peer-reviewed journals.
  • Prior experience working across multiple product lines, business units, or global project teams.
  • Demonstrated ability to drive continuous improvement through data-driven decision ma
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