Senior Manager, Supply Planning

🕒 September 22

🇺🇸 United States – Remote

💵 $180k - $195k / year

⏰ Full Time

🟠 Senior

👔 Manager

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Iovance Biotherapeutics, Inc.

WebsiteLinkedInAll Job Openings

501 - 1000 employees

Founded 2014

🏥 Healthcare

🧬 Biotechnology

💊 Pharmaceuticals

Healthcare • Biotechnology • Pharmaceuticals

Iovance Biotherapeutics, Inc. is pioneering a transformational approach to treating cancer by harnessing the human immune system's ability to recognize and attack diverse cancer cells in each patient. The company focuses on T-cell-based immunotherapy, specifically Tumor Infiltrating Lymphocyte (TIL) therapy, which involves reinvigorating a patient’s TILs to fight cancer. Iovance's TIL therapy is being investigated in clinical trials across multiple advanced solid tumor cancers. Additionally, the company is advancing genetically modified TIL therapies and exploring potential applications of PBL (peripheral blood lymphocyte) therapy for blood cancers. As a leader in cell therapy, Iovance owns a state-of-the-art Cell Therapy Center in Philadelphia for manufacturing their therapies using proprietary GMP. The company is at the forefront of developing personalized and patient-specific cancer treatments.

📋 Description

• Design, develop, and implement clinical supplies strategies for clinical trials • Oversee labeling, packaging, release, distribution, and returns of clinical supplies at external CMOs • Maintain budgets and ensure projects are delivered on time • Create and manage clinical forecast plans and budgets for multiple programs and study levels • Create global supply strategies and plans for clinical studies • Collaborate with Clinical Operations, Regulatory Affairs, Quality Assurance, and external vendors • Support new site onboarding and manage forecasting and distribution of co-therapy drugs in the US and ex-US • Manage clinical trial supply, IMP production, inventory, and worldwide distribution to ensure uninterrupted supply • Manage label development from master label text through printing • Implement scheduling software for clinical trials and future commercial requirements, including chain of custody, identification, real-time scheduling, and tracking • Manage development, review, and User Acceptance Testing of the Interactive Response Technology system • Review manuals and documents with the Clinical Operations team • Represent Supply Planning at clinical trial team meetings and communicate plans and timelines • Partner with CMC, Regulatory Affairs, Clinical Operations, and Quality Assurance leaders • Present recommendations to Senior Tech Ops, Clinical, and Commercial leadership • Perform other duties as assigned

🎯 Requirements

• Bachelor’s degree in a related field • 5+ years in a related supply chain/planning/operations role • Prefer prior experience planning in time critical and temperature sensitive products • Ability to work with multiple database and electronic systems • Experience with Oracle/ERP, courier, and material ordering portals, a plus • Strong analytical and problem-solving skills • Attention to detail • Outstanding organizational skills with the ability to multi-task and prioritize • Excellent interpersonal, verbal, and written communication skills, including presentations and ability to influence all levels of staff, including executives • Experience in writing SOPs • Advanced qualitative and quantitative analytical skills • Good business acumen, strategic and analytical thinking, including financial analysis • Ability to balance multiple priorities in a fast-paced environment while delivering timely, high-quality work • Skilled with Microsoft Excel and PowerPoint • Ability to sit for extended periods in front of a computer

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