Jobs at ImmunityBio

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.

The Principal Statistical Programmer manages statistical programming for clinical trial data, ensures quality and compliance for CDISC standards, and mentors junior staff.

Provide legal support for clinical trials by drafting, reviewing, and negotiating CTAs and related agreements; advise on regulatory, data privacy, IP, indemnification, and payment terms; develop templates, playbooks, and policies; manage vendor/CRO contracts; ensure compliance with FDA, GCP, HIPAA, GDPR; support due diligence and CLM improvements.

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.