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The Director of Pharmacovigilance at Arcellx is responsible for overseeing safety governance and management for all products, leading departmental SOP development, and ensuring timely assessment of individual case safety reports. This role includes strategic leadership of pharmacovigilance functions and collaboration with cross-functional teams while representing PV in audits with health authorities.

As a Senior Manager, Market Planning, you'll lead market research and competitive intelligence efforts, collaborating with commercial teams to drive strategic decisions for anito-cel's launch. You will gather insights from stakeholders, analyze data, and provide updates on treatment landscapes and competitive threats, ensuring effective market strategies pre- and post-launch.

The Associate Scientist will design and execute bioanalytical experiments, optimize workflows, develop assays, analyze clinical samples, and support cross-functional teams with data interpretation and report preparation.

The Senior Manager, Pipeline Strategy will lead drug development strategies, manage pipeline projects from clinical candidate nomination through proof of concept, oversee preclinical data updates, and ensure project alignment among cross-functional stakeholders to maximize clinical and commercial success.

The Director of Biostatistics will lead statistical discussions, provide strategic input for clinical documents, and mentor junior statisticians. They will oversee biostatistics teams to ensure high-quality deliverables and collaborate with clinical teams to analyze study results and support publication tasks.

As a Scientist at Arcellx, you will execute protein and molecular biology engineering strategies, working with a team to design and develop therapeutic candidates for cancer therapies. You will engage in designing expression plasmids, conducting experiments, and communicating project progress effectively within a fast-paced environment.

The Principal QC Specialist will lead the development of a new QC testing laboratory and establish various quality management systems. Responsibilities include performing technical reviews, drafting SOPs, and coordinating equipment qualification while ensuring compliance with industry regulations.