Manager, Clinical Supply Chain

Job not on LinkedIn

🔥 0 minutes ago

🇺🇸 United States – Remote

💵 $66k - $169.4k / year

⏰ Full Time

🟡 Mid-level

🟠 Senior

🔗 Supply Chain

👻 Ghost score 0%

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Eli Lilly and Company

WebsiteLinkedInAll Job Openings

10,000+ employees

💊 Pharmaceuticals

🏥 Healthcare

🧬 Biotechnology

💰 $6.5M Post-IPO Debt - Eli Lilly on 2024-02

Pharmaceuticals • Healthcare • Biotechnology

Eli Lilly and Company is a multinational pharmaceutical company that researches, develops, manufactures, and markets prescription medicines across multiple therapeutic areas including diabetes, oncology, immunology, neuroscience, and pain. Headquartered in Indianapolis, Indiana, Lilly is known for its extensive R&D, clinical development, and global commercialization of biologic and small-molecule drugs. The company focuses on drug discovery, clinical trials, regulatory approvals, and large-scale pharmaceutical manufacturing and distribution.

📋 Description

• Contribute to the development and execution of clinical supply strategies for early- to mid-phase clinical trials (Phase 1–3 as applicable) • Manage clinical supply plans, demand forecasts, and inventory strategies, including tracking through Interactive Response Technology (IRT) systems • 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 to develop, review, and approve clinical labels • Support CDMO packaging/labeling schedules to ensure supply availability • Manage logistics and licenses required to ship materials from manufacturing to bulk storage facilities, courier depots, and investigator sites • Collaborate with CMC and QA to facilitate document transfer required for IP/QP release by CDMOs • Monitor shelf-life and expiry dating, and coordinate retest/extension activities • Manage investigations, reporting, and communication of temperature excursions and product complaints • Support product recovery activities pending investigation of IP from investigator sites • Communicate across functional areas regarding clinical supply chain processes • 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

🎯 Requirements

• Bachelor's degree in engineering or science required • 3–5 years of biotech/pharma industry experience in clinical supply chain, including international experience, required • 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, with 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

🏖️ Benefits

• 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 (ERGs) offering support networks