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The Principal Statistical Data Scientist will oversee multiple projects, ensuring deliverables meet CDISC aligned standards. They will validate datasets, execute code runs, support project requirements, and mentor junior team members while collaborating with global stakeholders on project goals.

The QA Coordinator is responsible for managing change control and document control systems at the KAEC site, ensuring compliance with GMP regulations and Pfizer standards. This includes overseeing training programs, coordinating documentation, and preparing reports related to training and process management.

The Senior Associate Scientist will support drug development efforts in oncology, utilizing immunological, cellular, and molecular biology techniques to investigate cancer biology and novel therapeutic targets. Responsibilities include executing laboratory methodologies, analyzing data, and collaborating with a cross-functional team.

The Oncology Research Project Leader is responsible for leading discovery and clinical-stage research teams, developing project strategies, managing risks, and facilitating decision-making across various stakeholders. This role involves mentoring junior leaders, ensuring regulatory compliance, and collaborating on project transitions to meet objectives.

The Senior Associate Scientist, Automation will design and develop laboratory automation solutions, integrating robotic systems and digital tools, while collaborating with a multi-disciplinary team to enhance workflows in pharmaceutical drug development.

As a Senior Associate Lab Automation Scientist, you will collaborate with diverse teams to develop and implement advanced automation and robotics in pharmaceutical R&D. Your role involves programming laboratory systems, integrating instrumentation, and enhancing workflows with digital tools and data analysis to improve efficiency and quality in drug development processes.