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US: Senior or Principal Biostatistician

Date: 25-Oct-2016
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Senior or Principal Biostatistician


Provide statistical expertise and leadership to project and analysis team. Provide statistical consulting and technical support as it relates to the design and statistical analysis of clinical studies. Determine analysis and data presentation specifications for SAS Programming staff. Perform analysis, interpret study results, and collaborate with medical and biostatistics staff to produce interim reports and final reports. May be responsible for more than one study.


Understanding of GCP, ICH, and FDA guidelines and regulations applicable to conduct clinical research. Experience with, and mastery of, statistical methods commonly used in the analysis of data obtained from Phase I IV clinical trials. Experience with SAS Base and SAS Stat, as well as strong data step skills. Experience with other statistical software packages, such as N-Query, S-Plus. Ability to work creatively and independently to carry out assignments of a complex nature. Ability to work effectively and cooperatively with other professional staff members. Ability to communicate effectively, both verbally and in writing, with all levels of staff and with the public.


Degree requirements include one of the following: Masters-level degree in Statistics, Biostatistics or related field with four years relevant work experience; total work experience to include one year in CRO industry or biotech; or Doctorate-level degree in Statistics, Biostatistics or related field with one year relevant work experience in CRO industry or biotech. Data handling and analysis experience. Excellent interpersonal and organization skills.

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