Senior or Principal Biostatistician

Skills / Requirements:

• PhD degree or equivalent, in Statistics or Biostatistics. Exceptional candidates with MS degree in Statistics or Biostatistics may be considered

• 3 years analyzing and interpreting clinical trials data and/or managing/QCing SAS programming in the Pharmaceutical & Biotech industry. Experience with additional programming languages is a plus.

• Solid ability in the design, analysis, and interpretation of clinical trials, particularly in time-to-event analyses, propensity score or other matching or weighting methods and/or Bayesian approaches to clinical trials with an appetite for innovation

• Familiarity with drug development life cycle and experience with the standardization, integration, analysis and reporting of clinical trials' data.

• Regulatory submissions knowledge and experience utilizing define.xml and other submission documents is a plus. Understanding of FDA guidelines.

• Strong SAS skills and knowledge of CDISC standard. Experience working with and guiding statistical programmers. Experience in Phase II/III Oncology trials a plus

• Excellent written and verbal ability, including the ability to be persuasive to a technical or non-technical audience

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.