WHO WE ARE

Arcellx is a public, clinical-stage biotechnology company reimagining cell therapy by engineering innovative immunotherapies for patients with cancer and other incurable diseases. We believe that cell therapies are one of the forward pillars of medicine and our mission is to destroy cancer and advance humanity by developing cell therapies that are safer, more effective, and more broadly accessible.
Our team members are made up of talented innovators and dreamers working from our offices in Rockville, Maryland, and Redwood City, California. At Arcellx, we hire exceptional people and create a fun, diverse, supportive, and informal environment that allows everyone to do their best work.

SKILLS AND EXPERIENCE WE LOOK FOR

• BS/BA degree in related discipline.
• 13+ years of experience in statistical programming with clinical data and SAS.
• Experience in oncology therapeutic area preferred.
• Strong SAS programming skills required with proficiency in SAS/Base, SAS/Stat and SAS/Macros.
• CDISC expertise required.
• Uses broad expertise or unique knowledge and skills to contribute to development of company objectives and principles, and to achieve goals in creative and effective ways.
• Excellent interpersonal communication skills.

• Provide oversight development of datasets (SDTMs/ADaMs) in CDISC compliant format by CROs.
• Review of SDTM mapping specifications, annotated CRFs, ADaM specifications, define XML documents and reviewers’ guides per CDISC and FDA specifications and guidelines.
• Provide technical leadership, problem solving of moderate to high complexity and within project timelines while providing high quality deliverables.
• Demonstrate expertise in SAS language, procedures, and options commonly used in clinical trial reporting including the Macro language, BASE SAS, SAS/STAT & SAS/GRAPH.
• Oversee and manage work of other programmers.
• Develop and/or validate standard macros to automate output production.
• Assist with infrastructure development of the department.