[I, Librarian]
  • [Photo] Sharie Sell • May 13, 2004

    BACKGROUND

    STATPROBE, Inc is one of the largest privately held CROs in the United States. We deliver high quality CRO services to the pharmaceutical, biotechnology, and medical device industries. We are experienced with nearly every therapeutic classification, with special expertise in oncology, CNS, endocrinology, cardiovascular, anti-infectives, virology and women's health. We are looking for a Senior Biostatistician to join our team in our Columbus, OH office.

    RESPONSIBILITIES

    Senior Biostatisticians oversee the development, progress, accuracy, and timely completion of research projects. They also plan, analyze, review, interpret and summarize the statistical component of research projects.

    Primary Responsibilities:
    • Determine schedule for projects, including deadlines, from initiation to final product
    • Determine amount of time to be spent on each stage of the project and identify individuals who will be responsible for completing tasks
    • Identify available resources for projects
    • Develop project analysis plan, including computer-generated table specifications, statistical analysis plan, and research report format
    • Assign tasks and provides necessary project materials to appropriate individuals, and discuss current workload and timelines with individuals
    • Verify statistical programs, statistical results, and data sets used in statistical section of technical documents
    • Write statistical section of technical documents, including protocols when requested
    • Specify statistical terms and procedures and defines equations for derived variables
    • Oversee progress and development of research reports
    • Review project status on regular basis, and prepare project summaries for weekly/monthly status meetings
    • Establish and maintain project notebook (including correspondence records)
    • Maintain client contact, under the direction of the Director, Biostatistics, according to schedule or as deemed necessary
    • Provide final quality assurance check of research report
    • Update knowledge in statistical concepts, methods, and techniques, and maintain state-of-the-art statistical applications in clinical research

    REQUIREMENTS

    Education:
    An M.S., M.A., or MPH in statistics, biostatistics, epidemiology or equivalent is required.

    Experience:
    A minimum of five years experience with the design and analysis of clinical trials or Equivalent work experience is required. Individual must also be able to demonstrate experience to effectively manage numerous projects simultaneously and direct staff efforts in an efficient manner. An equivalent combination of education and experience may be substituted.

    PREFERENCES

    Ph.D. in statistics/biostatistics

    LOCALE

    Beautiful Columbus, OH

    COMPENSATION

    Commensurate with education and experience. Comprehensive benefits package including 401(k) plan with company match.

    HOW TO APPLY

    Please send your CV to hr[at]statprobe.com. We encourage you to visit us online at http://www.statprobe.com to learn more about and view other career opportunities at STATPROBE.

    STATPROBE welcomes and celebrates diversity and is an EEO/AA employer.

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