Iovance Biotherapeutics is a biotechnology company pioneering tumor infiltrating lymphocyte (TIL) therapy for cancer patients. The company is a clinical-stage organization with a strong focus on innovation and collaboration in a fast-paced environment.
Support GCP/GCLP/GVP audits for investigational sites, internal systems, and clinical service providers, including planning, coordination, and reporting.
Assist with commercial inspections, inspection readiness activities, and GCP compliance tasks such as investigations and change controls.
Maintain a continuous improvement mindset and represent the Clinical Quality Assurance Team in cross-functional projects.
Manage end-to-end patient cases for TIL therapy from referral through post-infusion, serving as a primary contact and trusted advisor.
Collaborate with treatment centers, interdisciplinary care teams, and internal partners to coordinate tumor procurement, manufacturing, and time-sensitive milestones.
Identify and resolve barriers to therapy access, track critical milestones, and contribute to continuous improvement and site onboarding best practices.