The Associate Scientist will design, plan, and execute experiments for clinical studies, focusing on immunostaining and flow cytometry assays. Responsibilities include processing clinical trial samples, supporting biomarker assay development, preparing data summaries, and staying abreast of new technologies for innovative improvements.

The Associate Director, Supply Chain Operations at Arcellx will develop and manage the clinical supply chain for cell therapy, ensuring timely supply of clinical trial materials. Responsibilities include strategic planning, execution of operations, vendor management, compliance, financial stewardship, and process improvement.

As a Senior Scientist, you will lead efforts in machine learning-based protein design initiatives to develop new cell therapies. Responsibilities include collaborating with a diverse team to design novel proteins, implementing ML solutions for various protein engineering challenges, and communicating progress and recommendations across teams.

As an Executive Assistant, you will manage complex calendars, schedule meetings, coordinate travel arrangements, assist with organizing company events, and collaborate on special projects for the executive team.

As the Associate Director of Market Access, you will implement innovative market access strategies for the launch of anito-cel, a CAR T-cell therapy. Your role will involve developing the value proposition, collaborating with various teams, leading insights generation, and providing strategic input on pricing and distribution to ensure access for patients with relapsed refractory multiple myeloma.

As a QC Specialist, you will execute release testing for cell therapy products using various methods, perform environmental monitoring, draft SOPs, manage lab equipment maintenance, and contribute to GMP investigations.

You will lead the development and optimization of commercial data and platform infrastructure supporting sales, marketing, and market access for Arcellx's CAR T candidate. Responsibilities include overseeing data system implementations, managing analytics solutions, ensuring data governance, and enhancing user experience post-launch.

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 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.

The Director of Pipeline Strategy will lead drug development strategies, manage pipeline projects, and oversee preclinical data updates. This role involves collaboration with senior management and cross-functional teams to ensure project alignment, manage timelines, and assess project viability, ultimately aiming for clinical and commercial success.