The Uro Oncology Business Manager is responsible for driving clinical adoption of Anktiva within assigned territories by building relationships with LUGPA clinics, academic institutions, and IDN hospitals. They must execute sales strategies, educate healthcare providers on treatment protocols, and manage account performance to achieve territory goals.
The Medical Information Specialist manages global medical information inquiries for ANKTIVA and supports clinical trial eligibility processes. They are responsible for creating medical response documents, reporting adverse events to pharmacovigilance, and ensuring compliance with regulatory standards.
The Clinical Trials Manager oversees clinical study activities, including the development of study-related documents and site management. They provide daily guidance to clinical sites regarding protocol interpretation and safety compliance while supporting data monitoring and regulatory document collection.
The Field Reimbursement Manager provides education and support to providers regarding coverage, coding, billing, and financial assistance for therapeutic products. They serve as the regional market access expert, analyzing reimbursement challenges and collaborating with internal teams to support business objectives.
The Corporate Accounts Director develops and expands strategic relationships with key clients to drive the adoption of Anktiva and achieve revenue goals. This role manages contract negotiations, implements business plans, and serves as the primary interface between the company and large urology group practices.
The Clinical Implementation Director educates healthcare providers on the safe and effective adoption of Anktiva while guiding practices in operationalizing the therapy within clinical workflows. This role involves identifying clinical barriers, supporting patient identification, and collaborating cross-functionally to ensure successful site onboarding and delivery.
The Senior Clinical Trials Manager is responsible for managing global clinical studies, including assisting with study-related documentation and site management. They provide daily guidance to clinical sites regarding protocol interpretation and safety compliance while overseeing site recruitment and data monitoring.
The DevOps Engineer will architect and maintain automated infrastructure and CI/CD pipelines to ensure reliable, scalable, and secure production services. They will collaborate with cross-functional teams to implement observability solutions and embed security best practices throughout the development lifecycle.
The Event Manager is responsible for planning, executing, and managing all aspects of medical and marketing events, including conferences and educational programs. They must ensure all activities comply with pharmaceutical industry regulations while aligning with strategic marketing objectives.
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.
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.
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.
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 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 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.
