arcusbiosciencescareers

Summary The Quality Assurance (QA) department is seeking an experienced QA professional who will be responsible for assessing, improving and maintaining the Quality Management System (QMS). This is to ensure a state of cGMP compliance and support the effective execution of Quality Management Systems

At Arcus, the Director, Clinical Pharmacology (CP) functions as the Clinical Pharmacology (CP) team representative at the project teams for small molecule and biotherapeutics in Phase 1-3 of clinical development and is responsible for supporting all clinical pharmacology-related activities. This inc

SummaryThe Biology department is seeking a self-motivated, knowledgeable, and technically skilled immunologist with a deep understanding of inflammatory and autoimmune disease mechanisms. In this role, you will design, execute, and interpret experimental studies to demonstrate the mechanism of actio

This role oversees site contracts, grants and payments to full‑service CRO partnerships responsible for operational execution of budgets, payments, reconciliation, and study financial controls. It maintains ensures just‑in‑time CRO funding, and supports accruals, reconciliation, and inspection‑readi

Summary The Clinical Trial Manager (CTM) will provide clinical study support to the Clinical Program Manager/Study Management Team Lead (SMTL) for one or more clinical studies, ensuring efficient delivery of clinical trials in a matrix environment. Key accountabilities include assuring successful co

Summary We seek a strong technical problem solver and decision maker to join our analytical team and help us achieve our goals for NDA readiness. This onsite role will be a key contributor to Arcus’ Pharmaceutical Development & Manufacturing organization. You are a hands-on expert in HPLC method dev

Summary The Director, Clinical Operations serves as a core member of the Product Development Team in the role of a Clinical Program Director (CPD) and is responsible for development of the operational strategic plans for the clinical trials within the assigned program. This includes contributing to