Senior Statistician – Clinical Biostatistics Late Development

Janssen Research & Development, LLC, a Johnson and Johnson Company, a member of Johnson & Johnson's Family of Companies, is recruiting for Principal Statistician. To be located in one of the following locations: Titusville, NJ USA, Raritan, NJ USA or Spring House, PA USA, or Belgium-Antwerp-Beerse.

At the Janssen Pharmaceutical Companies of Johnson & Johnson, what matters most is helping people live full and healthy lives. We focus on treating, curing and preventing some of the most devastating and complex diseases of our time. And we pursue the most promising science, wherever it might be found.  


Janssen Research & Development, LLC discovers and develops innovative medical solutions to address important unmet medical needs in oncology, immunology, neuroscience, infectious diseases and vaccines, and cardiovascular and metabolic diseases. Please visit for more information. 


We are Janssen. Our mission drives us. Our patients inspire us. We collaborate with the world for the health of everyone in it.


The Quantitative Sciences organization integrates Clinical and non-Clinical Biostatistics, Clinical Pharmacology, and Model Based Drug Development in a single aligned organization as part of Janssen Research & Development. We work in cross-disciplinary Quantitative Sciences teams and apply quantitative principles across the R&D portfolio to enable optimal decision-making at the earliest time point and in the most efficient manner.


We are specifically looking for a Senior Statistician to work in the Clinical Biostatistics Late Development group. The disease areas that are targeted are HIV and hepatitis.


The candidate should be able to:

  • Gain a thorough understanding of the safety, efficacy, the pharmacokinetics and the pharmacodynamics of one or more investigational compounds.
  • Contribute to the design and analysis of clinical trials in close collaboration with other Quantitative Sciences and Clinical Team members.
  • Have the ability to understand and apply innovative designs and analysis methods and support their evaluation via analytical studies and other appropriate methods.
  • Knowledge and experience in regulatory submissions is required.

  • Ph.D. in Statistics or related field with minimum 2+ years of relevant experience, or Master’s Degree in Statistics or related field with 4+ years of relevant experience is required.
  • Experience with antiviral drug development, in the HCV (Hepatitis) disease area is preferred.
  • Proficiency in SAS or R programming is required.
  • Basic knowledge of regulatory guidance documents such as ICH guidance is required.
  • Experience in developing clinical trial protocols is required.
  • Experience in planning and execution of statistical analyses for HA dossier and publications is required.
  • Experience producing clinical biostatistics top line reports is preferred.
  • Proven ability to work effectively within a geographically and culturally diverse work environment is required.
  • Travel up to 10% both domestic and international will be required.

Primary Location
United States-New Jersey-Titusville
Other Locations
North America-United States-Pennsylvania-Spring House, North America-United States-New Jersey-Raritan, Europe/Middle East/Africa-Belgium-Antwerp-Beerse
Janssen Research & Development, LLC. (6084)
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