Teva Pharmaceuticals USA, Inc.

Principal Statistician

US-PA-Great Valley
Requisition #
17-20330
# Positions
1
Category
Biostatistics

Overview

 

Principal/Senior Principal Statistician

Position Summary

The Principal/Senior Principal Statistician position is for a skilled statistician with training and experience in statistics. He or she is expected to provide statistical support to clinical studies within Teva Global R&D. The support includes, but not limited to, study designs and data analyses. He or she needs to be knowledgeable about statistical principles and appropriate software and tools to perform his or her tasks. A Principal/Senior Principal Statistician should be a strong individual contributor, beginning to demonstrate leadership qualities and creative and strategic thinking and capable and committed to developing over time into a leadership role. He or she must have excellent written and oral communication skills.  This position can be located in our Malvern, PA or Israel locations.

 

 

 

Responsibilities

Essential Functions:

 

  • Responsible for statistical aspect of study designs and data analyses from clinical studies
  • Provides study design input and consultation for clinical endpoint assessments and sample size planning for clinical studies
  • Prepares the preparation of statistical sections of clinical protocols in collaboration with Clinical Pharmacology personnel and/or Clinical Research, as deemed necessary
  • Writes, or oversees the writing of, statistical analysis plans
  • Works with Data Management and Clinical Research personnel to provide statistical input for CRF design
  • Conducts analyses to support clinical study reports, abstracts, manuscripts and other documents to support the marketing of Teva Global R&D products
  • Conducts analyses and document preparation to support global regulatory submissions, including briefing packages, integrated analyses and regulatory responses.
  • Collaborates with outsourcing partners and oversees conduct of statistical aspects of outsourced studies, as appropriate
  • Proactively assess and identify processes that require improvement
  • Participate in department initiatives to further the effectiveness of global statistics
  • Learn innovative and cutting-edge clinical trial design, methodology and analysis

Qualifications

Requirements:

  • Requirements:

    • PhD. in Statistics/Biostatistics (or related field) with a minimum of 3 years of related experience (senior principal statistician) or 0 years of related experience (principal statistician)
    • Excellent presentation and written communications skills.
    • Ability to communicate with non-statisticians to interpret statistical findings
    • Good organizational and problem-solving skills.
    • Demonstrated project and technical leadership qualities, and creative and strategic thinking required.
    • Ability to program using SAS, knowledge of R is beneficial

     

 

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