Manager, Clinical Supply Chain

🕒 il y a 1 mois

🇺🇸 États-Unis – Télétravail

💵 $105 000 - $169 400 / an

⏰ Temps Plein

🟡 Intermédiaire

🟠 Senior

🔗 Responsable Supply Chain

🗣️🇺🇸🇬🇧 Anglais requis

D'où vient cette offre

Publiée sur la page carrières de Eli Lilly and Company, pas via un site d'emploi

Repérée par Remote Rocketship il y a 1 mois

Logo of Eli Lilly and Company

Eli Lilly and Company

10 000+ employés

💊 Pharmaceutique

🏥 Santé

🧬 Biotechnologie

💰 €6 500 000 Post-IPO Debt - Eli Lilly en 2024-02

Pharmaceuticals • Healthcare • Biotechnology

Eli Lilly and Company est une entreprise pharmaceutique multinationale qui recherche, développe, fabrique et commercialise des médicaments sur ordonnance dans plusieurs domaines thérapeutiques, y compris le diabète, l'oncologie, l'immunologie, les neurosciences et la douleur. Basée à Indianapolis, dans l'Indiana, Lilly est reconnue pour sa vaste R&D, le développement clinique et la commercialisation mondiale de médicaments biologiques et de petites molécules. L'entreprise se concentre sur la découverte de médicaments, les essais cliniques, les approbations réglementaires et la fabrication et distribution pharmaceutique à grande échelle.

Description

• Support end-to-end planning, execution, and maintenance of uninterrupted clinical supply, including investigational product, comparators, and ancillary materials • Develop and execute clinical supply strategies for early- to mid-phase clinical trials, including Phase 1–3 as applicable • Manage clinical supply plans, demand forecasts, and inventory strategies through IRT systems in alignment with protocols and enrollment projections • Support packaging, labeling, distribution, and resupply activities for investigational products and comparators • Ensure on-time delivery of clinical supplies to depots and clinical sites globally • Partner with Quality, Clinical, CMC, and external CDMOs on clinical labels and packaging/labeling schedules • Manage logistics and licenses required to ship materials from manufacturing to storage facilities, courier depots, and investigator sites • Collaborate with CMC and QA on document transfer for IP/QP release by CDMOs • Monitor shelf-life and expiry dating and coordinate retest/extension activities • Manage investigations, reporting, and communication related to temperature excursions and product complaints • Support product recovery activities from investigator sites • Author Pharmacy Manuals for clinical studies as needed • Represent Supply Chain in Clinical and CMC Sub-Team meetings • Report to the Senior Director, Clinical Supply Chain

🎯 Exigences

• Bachelor's degree in engineering or science required • 3–5 years of biotech/pharma industry experience in clinical supply chain, including international experience, required • Must be authorized to work in the United States on a full-time basis • Lilly will not provide support for or sponsor work authorization or visas • Working knowledge of clinical supply chain processes and GMP/GDP requirements • Experience coordinating cross-functional project teams and external vendors • Strong organizational, analytical, decision-making, and interpersonal skills • Excellent attention to detail • Ability to work independently in a fast-paced, dynamic environment • Demonstrated ability to coordinate CDMO activities supporting clinical development of pharmaceutical products • Ability to thrive in a small-company culture and contribute to creating and implementing processes

🏖️ Avantages

• Company bonus, depending in part on company and individual performance • Company-sponsored 401(k) • Pension • Vacation benefits • Medical, dental, vision, and prescription drug benefits • Flexible benefits, including healthcare and/or dependent day care flexible spending accounts • Life insurance and death benefits • Time off and leave of absence benefits • Well-being benefits, including employee assistance program, fitness benefits, and employee clubs and activities • Employee resource groups and support networks

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