A company is looking for a Biostatistician.
Key Responsibilities
Provide statistical support in protocol development for observational studies and clinical trials
Author and review statistical analysis plans, analysis dataset specifications, and TFL shells
Conduct programming and analysis for Medical Affairs and RWE studies
Required Qualifications
PhD or MS in Biostatistics or Statistics
Minimum 4 years of experience in the pharmaceutical industry with statistical input into study design and analysis
Experience with Phase-4 studies, Medical Affairs studies, Real World Evidence (RWE), or HEOR studies
Proficiency in statistical software, SAS and R
Experience with SDTM and ADaM data standards
Biostatistician • Garden Grove, California, United States