Search the 10 jobs at Arcellx

The Director of Pharmacovigilance will lead the safety governance oversight for Arcellx products, manage PV-related activities performed by vendors, develop departmental SOPs, and ensure compliance with safety and pharmacovigilance regulations. The role includes cross-functional collaboration, aggregation of safety reports, and representation in audits.

As an Associate Scientist, you will design, execute, and optimize bioanalytical experiments for clinical studies, focusing on immuno-assays and sample analysis. You will interpret data to aid clinical developments and prepare reports for cross-functional teams while maintaining lab standards and equipment management.

The Director of Biostatistics will lead and guide statistical discussions for clinical programs, collaborate with project teams, author statistical analysis plans, perform data analysis, oversee biostatistics teams, and mentor junior statisticians, especially in the oncology space.

The Senior Manager of Pipeline Strategy will craft and deliver drug development strategies, manage pipeline projects from nomination through proof of concept, and oversee key preclinical data updates. This role requires cross-functional collaboration to ensure alignment and timely decision-making, ultimately supporting the success of clinical and commercial initiatives.

As an Associate Scientist, you will support Arcellx's drug pipeline by handling primary human immune cells, conducting in vitro immune assays, analyzing lentiviral quality, and performing various laboratory protocols. Your work is crucial to the discovery and optimization of cell-based therapies.

As a Scientist at Arcellx, you will execute protein and molecular biology engineering strategies within the Discovery group, collaborating with a team to design and express recombinant proteins for cancer therapies, and communicate project progress.

The Senior Analytical Scientist I will serve as a biophysics SME in CMC activities, conducting pre-formulation studies, formulation development, and product characterization. Responsibilities include collaborating on biophysical characterization, designing stability studies, troubleshooting analytical assays, and reviewing technical documents.

The Principal QC Specialist will develop and build a new QC testing laboratory, establish sample management systems, perform technical reviews of GMP methods, draft QC-related documents, and lead QC GMP compliance activities.

The Director of Pipeline Strategy at Arcellx will manage pipeline projects from candidate nomination through clinical proof of concept, guiding drug development strategies, overseeing preclinical data, and ensuring effective collaboration with cross-functional stakeholders to maximize success.

As a Principal Scientist on the Translational team, you'll be responsible for driving the development and execution of translational strategy for projects moving from discovery to early clinical development, with a focus on hematologic malignancy programs. You'll lead the implementation of clinical biomarker strategies, communicate translational updates, define novel mechanisms of resistance, and contribute to preclinical to clinical translation of pipeline assets.