Senior CMC Data Scientist
We have a current opportunity for a Senior CMC Data Scientist on a permanent basis. The position will be based in Colorado. For further information about this position please apply.
Position Summary
We are seeking a seasoned Senior CMC Data Scientist with a passion for transforming complex data into actionable insights that accelerate life-saving therapies. This individual will bring deep statistical expertise across Analytical Development and Quality, playing a pivotal role in CMC decision-making. The ideal candidate thrives in fast-paced environments, excels at building reproducible data products, and is driven by the mission to expand access to critical treatments in Car T Cell Therapies.
Core Accountabilities
Key responsibilities include:
Statistical Strategy & Regulatory Engagement
Develop and lead statistical strategies for process validation and comparability, including risk-based PPQ approaches. Serve as a direct interface with FDA/EMA statisticians during regulatory reviews.Study Design & Process Optimization
Design and analyze statistically robust studies to optimize manufacturing processes, define control strategies, and support regulatory submissions in alignment with ICH/FDA/EMA guidance.Data Product Development
Build and maintain reproducible data science products-such as interactive dashboards and analytic reports-that effectively communicate complex findings to diverse stakeholders.Collaborative Coding Practices
Work within Git-based workflows for version control and collaborative code development.Scientific-Computational Translation
Translate scientific questions into computational solutions by applying appropriate statistical models and methods.Cross-Functional Collaboration
Partner with scientists across disciplines including immunology, molecular biology, process development, and manufacturing.GMP Compliance
Adhere to GMP requirements as dictated by project needs, including timely completion of relevant training provided by Umoja.
Qualifications
Required:
- PhD (2+ years) or MS (5+ years) in Statistics, Biostatistics, Computer Science, Bioinformatics, or a related computational field.
- Strong foundation in applied statistics, modeling, and method selection.
- Proven experience solving computational problems in scientific research settings.
- Demonstrated ability to develop analysis pipelines and reports.
- Experience collaborating in therapeutic development, with fluency in both scientific and computational domains.
- Expertise in manufacturing statistics (e.g., process variability, specification setting, quality metrics).
- Advanced proficiency in R or Python.
- Practical experience with Git workflows.
Preferred:
- Familiarity with data engineering and cloud platforms (e.g., AWS).
- Experience with:
- Interactive dashboard/report development (e.g., R Markdown, Jupyter, Shiny, Dash, Streamlit).
- Omics assays (e.g., transcriptomics, proteomics, single-cell analysis, flow cytometry).
- AI/ML application development.
- Background in immunology and immune cell biology.
- Understanding of molecular mechanisms in cancer and cell therapy.
- Prior experience in biopharmaceutical R&D.
- Self-motivated with a track record of identifying and executing high-impact initiatives.
- Comfortable working independently while thriving in multidisciplinary teams.
- Proactive in improving workflows and accelerating project timelines.