Support clinical trial operations through protocol interpretation, document collection and TMF maintenance, site start-up and training, supplier coordination, IP and specimen tracking, invoice reconciliation, and cross-functional collaboration to ensure compliant, efficient study conduct.

The Clinical Implementation Director supports healthcare providers in adopting Anktiva, focusing on education, operational integration, and clinical workflow alignment while ensuring compliance with regulations.

The Contracts Counsel will manage vendor and corporate contracts, support procurement and business operations, and provide legal advice on clinical and commercial matters.

The Clinical Research Associate will support clinical research studies by managing documentation, training, communication, and ensuring compliance with protocols.

Responsible for supporting clinical trial administration, ensuring compliance with regulations, organizing study documents, and collaborating with trial teams to meet research goals.

The Clinical Trials Manager oversees multiple clinical studies, manages site activities, develops essential study documents, and ensures protocol compliance and safety. They also support site recruitment, training, and data management.

Manage global clinical studies, assist in document development, site management, compliance guidance, and staff training.

The Clinical Data Manager oversees clinical trial databases, creates documentation, reviews data, trains staff, and ensures compliance with regulatory standards.

The Senior Clinical Data Manager oversees clinical trial databases, mentors junior staff, and ensures data quality and compliance with regulatory standards.

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

The Talent Acquisition Partner will manage full-cycle recruiting while ensuring compliance, sourcing candidates, conducting interviews, and managing onboarding for ImmunityBio.