Key responsibilities: Provide input to clinical study design and protocol preparation, including power and sample size calculation Prepare statistical analysis plans and provide statistical interpretation for study report preparation Conduct inferential statistical analyses. Identify and resolve statistical issues. Research and stay current with innovated statistical methodologies Advise clients in drug approval and submission process and interact with regulatory agencies Supervise and mentor junior statisticians Qualifications and skills: PhD degree in statistics/biostatistics with 5+ years or MS degree with 7+ years of experience in the pharmaceutical/biotech industry or life science research Experience with SAS statistical programming for clinical studies is required Highly motivated. Good interpersonal and communication skills #J-18808-Ljbffr Pharmapace
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