The Commercial Counsel provides legal advice for commercial activities and ensures compliance with regulations for Arcellx products, overseeing contract review and promotional materials.

The Senior Scientist will develop and manage clinical biomarker assays, ensuring compliance and integrating new technologies while interpreting data and supervising others.

The Office Manager oversees daily operations, supports executive staff, manages facilities, tracks Purchase Orders, and coordinates events and travel.

The Associate Director will manage the clinical supply chain, ensuring timely supply of trial materials while developing strategies, overseeing operations, and fostering vendor relations for Arcellx's cell therapy pipeline.

Execute GMP-compliant testing for cell therapy products, manage lab supplies and equipment, support investigations, and track QC data.

Lead and inspire a sales team for the launch of a CAR T therapy, develop sales strategies, and build relationships with key stakeholders.

Lead and build a sales team for the launch of an innovative cancer treatment, developing sales strategies to drive adoption and performance.

The Senior Division Manager will lead a sales team, develop strategies for product launch, build customer relationships, and ensure compliance.

As a Senior Division Manager, you'll lead a sales team to launch cell therapy products, develop sales strategies, and drive market adoption.

The Senior Division Manager will build and lead a sales team to launch a cell therapy treatment, develop sales strategies, and drive market adoption.

Lead a sales team to launch a cancer treatment, executing strategies, managing performance, and building customer relationships to drive product adoption.

The Executive Assistant supports the Commercial team by managing calendars, coordinating meetings, facilitating travel, and ensuring efficient operations.

The Sr. Director, Public Relations will develop and execute communication strategies, manage media relations, and support executive leaders in conveying company objectives.

Manage QA operations during manufacturing, ensuring compliance with cGMP, conducting batch record reviews, and overseeing quality assurance processes.

As an Associate Scientist, you will support protein engineering efforts by designing and characterizing proteins for cancer therapy, collaborating with cross-functional teams.

The Supply Chain Associate will manage site qualifications, coordinate patient logistics, oversee inventory levels, and collaborate with cross-functional teams to ensure compliance and operational efficiency.

The Principal Scientist will lead translational strategies for clinical programs, integrating biomarker data to inform clinical decisions and ensure compliance with regulatory standards.

The Director of Investor Relations will develop and execute a strategic IR program, manage communications, support events, and collaborate with senior executives and financial communities.

The Manager will lead corporate communications and digital media efforts, curate content, manage editorial calendars, and engage audiences across multiple platforms.

The Senior Director, Statistical Programming oversees design and delivery of statistical programming solutions for clinical trials, ensuring CDISC compliance and managing programming teams.