

Principal Statistician - Real World Analytics
β - Featured Role | Apply direct with Data Freelance Hub
This role is for a Principal Statistician - Real World Analytics on a long-term, 2-year contract, offering $84.50-$98.60 per hour. Requires a PhD or MS in Biostatistics/Statistics, 4+ years in the pharmaceutical industry, and expertise in SAS, R, and RWE methodologies.
π - Country
United States
π± - Currency
$ USD
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π° - Day rate
784
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ποΈ - Date discovered
September 27, 2025
π - Project duration
More than 6 months
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ποΈ - Location type
Unknown
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π - Contract type
Unknown
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π - Security clearance
Unknown
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π - Location detailed
United States
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π§ - Skills detailed
#Programming #Datasets #Statistics #SAS #ADaM (Analysis Data Model) #ML (Machine Learning) #R
Role description
Pay Range $84.50-$98.60 per hr.
Long term 2 year contract
Core Essential Skill sets:
1. Education: PhD or MS in Biostatistics or Statistics
1. Experience in pharmaceutical industry to provide statistical input into the study design, statistical analysis, and reporting of interventional and observational studies.
1. Min 4 yrs experience with Phase-4 study, Medical Affairs study, Real World Evidence (RWE) or HEOR study.
1. Min 4 yrs experience in statistical software, SAS and R.
1. Min 4 yrs experience with SDTM and ADaM data standards.
1. Min 4 yrs experience with Real World Data (RWD) and RWE methodologies, such as propensity score analysis, causal inference.
1. Min 4 yrs experience with advanced statistical models such as mixed effect model approaches for repeated measures, Machine Learning (ML) methods.
Position Summary:
β’ Provide statistical support in protocol development for observational studies and/or clinical trials.
β’ Author and review of statistical analysis plans, analysis dataset specifications, and TFL shells.
β’ Work with programming and other cross-functional teams in Phase-4 non-interventional study to develop CRF, validate and review the datasets and results.
β’ Conduct programming and analysis for Medical Affairs, RWE studies.
β’ Support develop abstract, poster and manuscript as deliverables.
Pay Range $84.50-$98.60 per hr.
Long term 2 year contract
Core Essential Skill sets:
1. Education: PhD or MS in Biostatistics or Statistics
1. Experience in pharmaceutical industry to provide statistical input into the study design, statistical analysis, and reporting of interventional and observational studies.
1. Min 4 yrs experience with Phase-4 study, Medical Affairs study, Real World Evidence (RWE) or HEOR study.
1. Min 4 yrs experience in statistical software, SAS and R.
1. Min 4 yrs experience with SDTM and ADaM data standards.
1. Min 4 yrs experience with Real World Data (RWD) and RWE methodologies, such as propensity score analysis, causal inference.
1. Min 4 yrs experience with advanced statistical models such as mixed effect model approaches for repeated measures, Machine Learning (ML) methods.
Position Summary:
β’ Provide statistical support in protocol development for observational studies and/or clinical trials.
β’ Author and review of statistical analysis plans, analysis dataset specifications, and TFL shells.
β’ Work with programming and other cross-functional teams in Phase-4 non-interventional study to develop CRF, validate and review the datasets and results.
β’ Conduct programming and analysis for Medical Affairs, RWE studies.
β’ Support develop abstract, poster and manuscript as deliverables.