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Title:Associate Director, Biostatistics
Location:MA - Cambridge

This biostatistician will provide technical leadership to the department, partner with clinicians to design efficient trials, contribute to the development of clinical and regulatory strategies, and conduct clinical, PK/PD, and biomarker data analyses.

  • Design efficient clinical trials
  • Contribute to the development of clinical and regulatory strategies
  • Serve as an influential statistical consultant to clinical, regulatory affairs, commercial, translational medicine, and clinical pharmacology departments.
  • Provide technical advice to other biostatisticians
  • Perform clinical, biomarker and PK/PD data analyses
  • Write statistical analysis plan and reports
  • Perform statistical programming for advanced statistical analysis methods
  • Interact with FDA and other regulatory authorities as needed
  • Play a leadership role on project teams
  • Perform quality review of statistical analyses

  • PhD in Statistics with at least 5 years of pharmaceutical or biotech experience or 8 years of similar experience with a Masters degree.
  • Strong technical skills with demonstrated independent statistical research interest and skills
  • Profound understanding of advanced clinical trial designs
  • Ability to lead project teams, as well as work in a cross-functional team
  • Broad knowledge of medical and biological terminology
  • Good statistical programming skills
  • Ability to multitask and prioritize work
  • Excellent communication and interpersonal skills
  • Strong coaching and mentoring skills

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