Posted on Mar 17, 2019 by Hobson Prior
Lead statistical and programming study teams and perform statistical analyses of a variety of studies.
Coordinate and provide statistical oversight for outsourced studies, performing QC of the quality of the deliverables returned by external vendors and CROs.
Write statistical sections of protocols and statistical analysis plans.
Represent biostatistics within cross functional study teams and provide statistical support and solutions to these teams.
Provide statistical expertise in interactions with Health Authorities.
PhD or MSc Degree in Statistics, Biostatistics or related
Experience within the Pharmaceutical, Biotech or CRO sectors
Excellent programming skill in SAS. Experience using R is a plus
Knowledge of CDISC
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