Senior Manager, Supply Planning

Emploi pas sur LinkedIn

🕒 il y a 6 jours

🇺🇸 États-Unis – Télétravail

💵 $180 000 - $195 000 / an

⏰ Temps Plein

🟠 Senior

👔 Manager

👻 Score fantôme 0%

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🗣️🇺🇸🇬🇧 Anglais requis

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Logo of Iovance Biotherapeutics, Inc.

Iovance Biotherapeutics, Inc.

501 - 1000 employés

Fondée en 2014

🏥 Santé

🧬 Biotechnologie

💊 Pharmaceutique

Healthcare • Biotechnology • Pharmaceuticals

Iovance Biotherapeutics, Inc. est à la pointe d'une approche révolutionnaire pour traiter le cancer en exploitant la capacité du système immunitaire humain à reconnaître et attaquer diverses cellules cancéreuses chez chaque patient. La société se concentre sur l'immunothérapie basée sur les cellules T, plus précisément sur la thérapie des lymphocytes infiltrant les tumeurs (TIL), qui consiste à revitaliser les TIL d'un patient pour lutter contre le cancer. La thérapie TIL d'Iovance fait l'objet d'essais cliniques sur plusieurs cancers à tumeurs solides avancées. De plus, l'entreprise développe des thérapies TIL génétiquement modifiées et explore les applications potentielles de la thérapie par lymphocytes du sang périphérique (PBL) pour les cancers du sang. En tant que leader de la thérapie cellulaire, Iovance possède un centre de thérapie cellulaire de pointe à Philadelphie pour la fabrication de leurs thérapies en utilisant un GMP propriétaire. L'entreprise est à l'avant-garde du développement de traitements contre le cancer, personnalisés et spécifiques à chaque patient.

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

🎯 Exigences

• 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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