Contribute to clinical development of plan preparation; Review of study protocol and preparation of statistical methodologies; Programming of study analysis, review of study results and preparation of statistical methods section for clinical/statistical reports; Communicate project requirements for CRF design, database design and database cleanup to ensure the key study variables are suitable for analysis; and; Communicate statistical results to medical writing personnel to ensure accurate interpretation
Requirements:
Ph.D. degree in Biostatistics/Statistics with strong experience in SAS Programming or equivalent; and; 1-2 years of experience in a pharmaceutical or CRO setting preferred
Text:
Biostatistician (PhD) Contribute to clinical development of plan preparation; Review of study protocol and preparation of statistical methodologies; Programming of study analysis, review of study results and preparation of statistical methods section for clinical/statistical reports; Communicate project requirements for CRF design, database design and database cleanup to ensure the key study variables are suitable for analysis; and; Communicate statistical results to medical writing personnel to ensure accurate interpretation Ph.D. degree in Biostatistics/Statistics with strong experience in SAS Programming or equivalent; and; 1-2 years of experience in a pharmaceutical or CRO setting preferred
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