
Detail-oriented Biostatistics graduate student with experience applying statistical programming, data analysis, and automation in regulated pharmaceutical and manufacturing environments. Skilled in R, Python, SAS, SQL, and statistical modeling with hands-on experience supporting clinical trial workflows, regulatory submissions, data validation, and reproducible analytics. Proven ability to collaborate across cross-functional teams, automate reporting pipelines, and communicate complex statistical findings to technical and non-technical stakeholders. Strong interest in statistical applications for process optimization, experimental design, quality systems, and digital transformation in pharmaceutical manufacturing.
Statistical Methods:
Regression modeling, clinical trials, experimental design, predictive modeling, multivariate analysis, statistical inference, process monitoring, data validation
Pharmaceutical & Regulatory:
Clinical trial data review, CDISC, Definexml, GCP, regulatory submission support, audit trails, reproducible workflows
Programming & Analytics:
R, Python, SAS, SQL, Tableau, Excel
Platforms & Tools:
Snowflake, Databricks, Azure, Domino Data Lab, Linux/Unix, Agile workflows
Professional Skills:
Cross-functional collaboration, technical communication, process improvement, automation, stakeholder engagement, documentation, continuous improvement, project coordination