Teams at CRISPR Therapeutics

The Senior Engineer II leads the development and scaling of mRNA manufacturing processes, applying statistical analysis and collaborating with teams to ensure quality and efficiency in gene editing therapeutics.

Leads cross-functional biotechnology R&D programs from discovery through early clinical development. Develops integrated strategies, plans, timelines, milestones, and risk mitigations; drives alignment across preclinical, CMC, manufacturing, regulatory, clinical, commercial, and finance teams. Represents programs to senior management, facilitates issue resolution and decision-making, manages stakeholder and alliance communications, and improves program execution processes. Requires strong knowledge of gene editing, cell and gene therapies, biologics development, and early clinical and regulatory activities.

Develop, validate, and modify SAS programs to analyze clinical trial data; create and validate CDISC-compliant SDTM and ADaM datasets; implement edit checks and produce high-quality tables, figures, and listings; collaborate with Clinical Operations, Data Management, and Biostatisticians for timely FDA submissions.