Jobs at ImmunityBio

Manage day-to-day administration and support for GxP computerized systems, ensuring compliance with regulations and providing technical leadership for system deployments and upgrades.

Support QC stability and reference programs by scheduling tests, entering and trending data, performing basic statistical analysis, drafting protocols and reports, packing/shipping materials, maintaining logs and stability chambers, assisting regulatory submissions (IND/BLA), and supporting quality systems including SOP updates and change requests.

Serve as strategic HR partner to leadership, advising on employee relations, performance management, compensation, recruitment, training, policy compliance, and HR projects. Conduct investigations, report people metrics, and ensure alignment of HR practices with business objectives.

Temporary talent sourcing partner responsible for proactive candidate identification and pipeline development for specialized, hard-to-fill biotech roles. Partners with TA team to source passive candidates via LinkedIn Recruiter, talent databases, and industry networks; conducts talent mapping, outreach, preliminary qualification, and maintains ATS records while reporting sourcing metrics and improving sourcing effectiveness.

Serve as a QC analytical subject matter expert to advise on method development, validation, transfer, and troubleshooting. Author and review SOPs, test methods, IND/BLA analytical sections, CoAs, OOS investigations, and batch release documentation. Review stability and lot release data, manage change controls and supplier notifications, collaborate with QA/regulatory and contract testing labs, and support data trending and quality investigations.

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.

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.

Provide legal support for clinical research by drafting, reviewing, and negotiating Clinical Trial Agreements and related vendor and commercial contracts. Ensure compliance with FDA, GCP, HIPAA, GDPR and other regulations; develop templates, SOPs, and negotiation playbooks; advise internal stakeholders on risk mitigation; assist with informed consent review; deliver training and lead process-improvement and cross-functional projects.

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