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The Principal Biostatistician designs and analyzes early-phase clinical trials, applying statistical expertise to inform trial strategy and regulatory interactions. Responsibilities include leading study designs, ensuring quality statistical deliverables, and shaping clinical narratives based on complex data analysis.

The Principal Quality Control Specialist will oversee QC Master Data management in a GMP setting, lead investigations, develop training, and ensure compliance with quality standards.

The Computational Scientist will lead computer vision and AI/ML projects, develop machine learning algorithms for spatial omics data, and collaborate with researchers for data interpretation and visualization.

The Senior Digital Systems Analyst manages digital system capabilities related to SAP, overseeing requirements, testing, and deployment while ensuring GMP operations are unaffected. This role includes training coordination, dashboard management, and site communications regarding digital solutions.

The Expert Imaging Lead for CVRM leads therapeutic area imaging strategies, integrating AI and ML within clinical research and drug development, collaborating with cross-functional teams and external partners for scalable imaging solutions.

Lead the Manufacturing Science and Technology team to drive process validation, technology transfer, and laboratory operations for cell therapy manufacturing, ensuring compliance and innovation.

The Director will lead the Specialized Analytics team in biologics development, overseeing complex analytics, driving innovation, and ensuring quality and collaboration.

The Senior Director leads a team in Analytical Development, overseeing strategies and deliverables for biologics, ensuring compliance and managing cross-functional collaboration while supporting regulatory submissions.

The Senior Director leads a team in analytical characterization of biologics, overseeing strategies and advancing digital efforts in a fast-paced environment.

The role involves leading and mentoring a team in analytical development for biologics, managing projects, and supporting regulatory submissions.