The Senior Clinical Research Associate will execute all site monitoring visit types and drive high-quality clinical research through proactive risk management and protocol interpretation. They will also serve as a subject matter expert for clinical sites, ensuring data integrity and regulatory compliance throughout the study lifecycle.
The Associate Director will lead the company's Risk-Based Quality Management strategy and chair the Clinical Data Quality and Governance Board. They are responsible for overseeing central monitoring operations, managing multi-vendor data streams, and driving a proactive, risk-based approach to clinical data quality.
The Associate Director designs and oversees monitoring strategies, including Risk-Based Quality Management and Decentralized Clinical Trial components to ensure data integrity and regulatory compliance. They lead a cross-functional team of remote Clinical Research Associates and act as a primary liaison with CROs and site investigators.
Responsible for the configuration, maintenance, and optimization of the Workday system to ensure stability and data integrity. The role involves designing custom reports, supporting HR functions, and managing system updates and end-user support.
Proactively identify and engage highly qualified passive candidates to build strong talent pipelines for critical roles in biotechnology. Partner with Talent Acquisition teams to develop targeted sourcing strategies and conduct market research to identify specialized talent pools.
Act as the primary scientific resource for Key Opinion Leaders and healthcare practitioners to educate them on ImmunityBio products and disease states. Facilitate clinical research, gather field insights, and implement medical affairs strategic plans within the Northeast region.
Provide strategic and operational leadership for global clinical trial data management activities across Phase I–IV trials. Define enterprise-wide data governance strategies and oversee the delivery of high-quality, regulatory-compliant datasets for submissions and publications.
The Senior GCP Auditor ensures compliance with GCP standards, SOPs, and FDA regulations through internal and vendor audits. They are responsible for maintaining the Quality Management System and ensuring constant inspection readiness for clinical trials.
Lead all aspects of statistical programming, including the creation and validation of analysis datasets and statistical outputs for clinical trials. Oversee technical quality, ensure regulatory submission readiness, and mentor junior staff members.
The Senior Biostatistician serves as the subject matter expert for the design, management, and quality of statistical analyses for phase I-III clinical trials. Key duties include developing statistical analysis plans, writing methodology sections for protocols, and ensuring regulatory compliance for data submissions.
Serve as the primary statistical lead for complex clinical programs, overseeing study design, analysis, and regulatory submissions. Collaborate cross-functionally to develop protocols, SAPs, and ensure data standardization according to CDISC standards.
Act as the primary scientific resource for Key Opinion Leaders and healthcare practitioners to educate them on ImmunityBio products and disease states. Facilitate clinical research, gather field insights, and implement medical affairs strategic plans within a specific geographic region.
The Field Medical Director serves as a non-promotional scientific resource to Key Opinion Leaders and healthcare practitioners to educate them on products and disease states. They are responsible for implementing medical affairs strategic plans, facilitating clinical research, and gathering field insights to inform internal stakeholders.
Design, build, and maintain AI-driven full-stack web and mobile applications using modern frameworks and containerized deployments. Collaborate with cross-functional teams to integrate LLM frameworks and ensure secure, high-performance system scalability.
Design, develop, and deploy production-grade AI agent systems and RAG pipelines using frameworks like LangGraph and CrewAI. Collaborate with cross-functional teams to implement secure tool execution, observability, and comprehensive testing strategies.
Design, develop, and maintain responsive user interfaces for AI-driven web and mobile applications. Collaborate with backend teams to integrate APIs and maintain a unified design system across various platforms.
Design, develop, and deploy production-grade AI agent systems and FastAPI-based servers. Implement RAG pipelines, security guardrails, and observability tooling to ensure reliable AI operations.
The Senior Security Engineer will own the end-to-end security of AI systems, including threat modeling, adversarial testing, and implementing security controls across the ML lifecycle. They will collaborate with cross-functional teams to embed security into AI development pipelines and ensure compliance with regulatory frameworks.
The Senior Security Engineer will serve as the Subject Matter Expert for securing AI infrastructure, including model hosting and agent orchestration platforms. They will design and implement robust identity management, logging, and observability pipelines while ensuring compliance with security frameworks.
The Uro Oncology Business Manager is responsible for driving clinical adoption of Anktiva within assigned territories by building relationships with key healthcare providers and institutions. They must analyze account performance, execute sales strategies, and educate HCPs on treatment protocols and reimbursement.
The Uro Oncology Business Manager is responsible for driving clinical adoption of Anktiva within assigned clinics, hospitals, and academic institutions. They will build strong relationships with healthcare providers, manage territory strategy, and educate stakeholders on product efficacy and treatment protocols.
The Uro Oncology Business Manager is responsible for driving clinical adoption of Anktiva within assigned territories by engaging with LUGPA clinics, academic institutions, and IDN hospitals. The role involves executing sales strategies, managing account performance, and educating healthcare providers on treatment protocols and reimbursement.
The Senior Clinical Data Manager creates and reviews study-specific CRFs, configures, migrates, and tests EDC databases, and serves as the study database manager, compiling edit checks. They perform data review, query management, and coding of verbatim terms like adverse events and medications, collaborating with medical scientists.
The Uro Oncology Business Manager is responsible for driving clinical conviction of Anktiva and achieving performance results within their territory. This includes executing sales strategies, building customer relationships, and analyzing account performance to identify barriers to prescriber adoption.
