Senior Manager, Real-World Evidence (RWE) Biostatistician
Uxbridge, United Kingdom
GBP 80K-86K (estimate) Senior-level Full Time
Tasks
- Analyze and interpret RWE study results
- Author and review statistical analysis plans
- Author and review study protocols
- Author and review study publications
- Author and review study reports
- Communicate complex real world data to stakeholders
- Conduct exploratory data analysis
- Curate and assess real world data quality
- Define data requirements and analytical strategies
- Design and implement data pipelines
- Develop RWE study methodologies
- Ensure compliance with data governance privacy and regulatory standards
- Identify patient cohorts
- Maintain documentation for data sources and transformations
- Perform data summary analytics
- Transform raw real world data into analysis datasets
Perks/Benefits
Skills/Tech-stack
Clinical Trial Design | Clinical trial | Cohort identification | Data Analysis | Data Governance | Data Modeling | Data Pipelines | Data Quality | Data quality control | Exploratory Data Analysis | Healthcare Data | Healthcare data modeling | Privacy Compliance | Python | Quality Control | R | Real-World Data | Real-World Evidence | Regulatory Compliance | SAS | Statistical Analysis | Trial design
Education
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