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Title:Sr. Biostatistician
Location:NJ - East Hanover

The Sr. Biostatistician is responsible for all statistical aspects of individual clinical trials.

  • Be responsible for all statistical tasks on the assigned clinical trials, e.g., clinical trial design/planning, analysis plan, reporting activities, exploratory analyses and additional analyses to support publications and statistical consultation during the running phase.
  • Track clinical trial activities and milestones.
  • Ensure timeliness and adequate quality of all CIS deliverables for the assigned trials.
  • Follow processes and adhere tonproject specific standards as well as Health Authority requirements (SOPs, NIPS, Master Analysis Plan, GCP, and regulatory guidelines).
  • Establish and maintain sound working relationships and effective communication within the clinical trial team and the CIS team.
  • Participate in non-clinical project activities as needed.

  • Minimum requirements M.S. in Statistics with at least 3 years' of related experience, or Ph.D. in Statistics with limited or no experience.
  • Strong statistical skills and application of Biostatistics discipline
  • Knowledge of the SAS computer package
  • Good oral and written communication skills
  • Good team collaboration.
  • Required years of experience One (1) - Three (3) Years

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