[Next-Generation Sequencing Book]
  • [Photo] Ted Clark • January 23, 2007

    BACKGROUND

    When Amgen was founded in 1980, the company consisted of a few scientists working on a single lab bench in one building. Today, we are the world’s largest biotechnology company, with approximately 14,000 staff members worldwide – and growing.

    Amgen has pioneered the development of novel products based on advances in recombinant DNA and molecular biology and launched the biotechnology industry’s first blockbusters. To sustain our success, we aim to attract and retain the most talented people who are dedicated to our mission of serving patients. Together, we live the Amgen values as we create innovative, best-in-class therapeutics that dramatically improve people’s lives.

    RESPONSIBILITIES

    The Senior Associate Biostatistical Programmer will support the company's request based on clinical trial data working with Global Biostatisticians. They will write, test and validate software programs to produce SDF and analysis datasets and TLGs for inclusion within aggregate review, data analysis, ad hoc requests, and other communications. Additionally, will understand and execute department-level, program-level and study-level macros and utilities. Performs QC checking of software programs written by other programmers and manages software development, testing and release in a Unix environment. Participates in process improvement initiatives within Biostatistical Programming, Assist in the review of key safety-related documents produced by other functions (e.g. Global Safety, Clinical Data Management etc.

    Addtionally:
    • Write, test and validate program-level macros and utilities
    • Interface with outsourcing partners and vendors at project level
    • Provide support to and mentor junior programmers
    • Assist in the review of Amgen Policies, SOPs and other controlled documents
    • Assist with project and systems audits by Amgen CQA and external bodies, and respond to audit questions and findings
    • Provide input to and participate in intra-departmental and Global Biostatistics and Global Safety meetings
    • Promote and communicate awareness of biostatistical programming and the role of the Biostatistics department to internal and external customers, both scientifically and process oriented
    • Contribute to the continuous improvement of Global Biostatistics and Development.

    REQUIREMENTS

    BS/BSc degree in Statistics, Computer Science, Mathematics, or Life Sciences
    3 years Biostatistical Programming experience using the SAS System
    Working experience in SAS and S-plus both for unix and PC environment
    Work experience in Clinical Trials within a Pharmaceutical, Biotechnology, or Public Health industry setting

    PREFERENCES

    Candidates should be able to relocate to Seattle, Washington

    TERMS

    Full-time employment

    LOCALE

    Seattle, Washington - 98119

    COMPENSATION

    DOE, Full Benefits

    HOW TO APPLY

    Please apply directly through the career website req number amge-00024406
    Link: http://www.amgen.com/careers

    DEADLINE

    Position posted 1/22/07 asap

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