[Next-Generation Sequencing Book]
  • [Photo] Diane Roberts • November 3, 2003

    POSITION

    Biostatistician

    LOCALE

    NJ and PA positions

    TERMS

    6+ month contract positions

    DESCRIPTION

    Provide statistical expertise in the statistical analysis and review of clinical trial data, and the production of study and submission documents to support an important NDA.

    RESPONSIBILITIES

    Key responsibilities include, but are not limited to:
    • QC and validate analysis database, analysis or table programs, and analysis results
    • Participate in the writing and critical review of data and programming specs, validation plan, SAP, CSR, ISS/ISE, etc.
    • Participate in the design and preparation of submission data package.
    • Perform QC/QA procedures according to company standards and policies on work performed by other statisticians or programmers.
    • As necessary, develop, test, validate, document and execute software and/or systems using the currently endorsed tools or support of production activities.

    REQUIREMENTS

    The position requires at minimum a MS degree in statistics or related field, with 5 years pharmaceutical industry (including CRO) experience. SAS programming ability is desired.

    HOW TO APPLY

    Please contact Diane Roberts, Recruiter, Main Line Contract Services
    droberts[at]mlpers.com or 610-822-1282 or 610-822-1210 (fax)

    [Please reference Bioinformatics.Org when responding to this announcement.]

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