Manager, Clinical Supply Chain

🕒 Yesterday

🇺🇸 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 global pharmaceutical company that researches, develops, manufactures, and distributes prescription medicines and provides patient support services. The company focuses on life-changing medicines across conditions such as diabetes, cancer, Alzheimer’s disease, autoimmune disorders, dermatology, migraine, obesity, and sleep apnea; it runs clinical trials, offers LillyDirect pharmacy services, and emphasizes manufacturing quality, medication safety, and research into genetic medicines. Eli Lilly also provides patient resources, condition education, and access programs to help people find care and participate in trials.

📋 Description

• Contribute to clinical supply strategies for early- to mid-phase clinical trials (Phase 1–3 as applicable) • Manage clinical supply plans, demand forecasts, and inventory strategies using IRT systems • Align supply planning with protocol requirements and enrollment projections • Support packaging, labeling, distribution, and resupply activities for investigational products and comparators • Ensure on-time delivery of clinical supplies to global depots and clinical sites • Partner with Quality, Clinical, CMC, and external CDMOs on clinical labels and packaging/labeling schedules • Manage logistics and licenses for shipping materials from manufacturing to bulk 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 concerning 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

🎯 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 • Authorized to work in the United States on a full-time basis • 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

🏖️ Benefits

• Company bonus depending in part on company and individual performance • Company-sponsored 401(k) • Pension • Vacation benefits • Medical benefits • Dental benefits • Vision benefits • 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 and fitness benefits • Employee clubs and activities • Employee resource groups open to all employees