Jobs at ImmunityBio

The Uro Oncology Business Manager drives adoption of Anktiva in clinics and hospitals, builds relationships, and trains healthcare providers on treatment.

Configure, maintain, and optimize the company's Workday system (HCM, Compensation, Talent, Learning, Absence). Provide day-to-day support, troubleshoot data/system issues, build custom reports and dashboards, ensure data integrity, support updates/releases, and partner with HR on process improvements and change management.

Lead global clinical data management strategy and operations across Phase I-IV trials. Oversee CRF design, database builds, edit checks, data quality, governance, vendor/CRO relationships, regulatory inspection readiness, modernization (automation/AI), budgeting, and talent development to deliver regulatory-compliant clinical datasets.

The Uro Oncology Business Manager drives treatment adoption of Anktiva among clinics and hospitals handling early-stage bladder cancer patients. Responsibilities include executing sales strategy, building customer relationships, training healthcare providers on drug administration, analyzing account performance, and collaborating with company partners.

The Uro Oncology Business Manager drives clinical conviction and adoption of Anktiva, builds relationships with healthcare providers, and analyzes performance barriers to boost treatment adoption in their territory.

The Uro Oncology Business Manager drives clinical conviction of Anktiva, focuses on treatment adoption, and builds relationships with healthcare providers within their territory.

The Senior GCP Auditor ensures compliance with GCP standards and regulations in clinical trials, oversees audits, and manages quality systems.

The Senior Biostatistician will oversee statistical analyses and reporting of clinical trial data, ensuring quality and compliance with regulatory standards while mentoring junior staff.

Lead design and operation of the Central Monitoring Unit and RBQM strategy. Chair the Clinical Data Quality and Governance Board, integrate multi-vendor clinical data into a centralized surveillance engine, escalate systemic issues, drive CtQ-focused culture, manage and coach central monitors, and own CMU SOPs and risk tools to meet global regulatory expectations.