Description
Responsibilities:Responsible for overseeing all aspects of statistical planning and analyses for clinical programs; directs both internal and external SAS programming efforts related to the responsible clinical programs.
Skills:
- Minimum of 6-8 years experience in pharmaceutical or biotechnology industry.
- Must have experience preparing analysis programs for clinical trials phases I-III.
- Must have been primary statistician on at least one NDA/BLA. Must have sound knowledge of statistical applications for clinical trials.
- Excellent writing and communication skills, and knowledge and skills of programming important.
- Strong knowledge of and experience in clinical trials design.
- Very good knowledge of drug development regulations pertinent to trial design and statistical analysis
Education:
MA or Ph.D. in (Bio)statistics.
CANDIDATE MUST HAVE - Statistics or Biostatistics degree - A master level statistician with at least 8 years of experience in oncology or a Ph.D. statistician with at least 5 years of experience in oncology clinical trials.
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