Senior Manager, Clinical Supply Chain

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🔥 0 minutes ago

🍂 Massachusetts – Remote

🍂 Massachusetts – Remote

⏳ Contract/Temporary

🟠 Senior

🔗 Supply Chain

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Sigma Systems

WebsiteLinkedInAll Job Openings

201 - 500 employees

📡 Telecommunications

⚡ Energy

☁️ SaaS

💰 $11M Venture Round - Tribold on 2009-01

Telecommunications • Energy • SaaS

Sigma Systems is a software company that provides cloud-native, API-driven BSS/OSS, product catalog, CPQ and order orchestration solutions for communications service providers and energy/utilities companies. It offers modular, TMF-compliant components and managed services — including AI-enabled automation and data-driven tools — to help operators modernize billing, monetization, and customer fulfillment processes with a SaaS and cloud-focused delivery model.

📋 Description

• Manage end-to-end Clinical Supply Chain activities, including planning, packaging and labeling, distribution, returns, and destruction, for assigned clinical programs • Develop and manage supply forecasts, supply plans, and timelines with Clinical and CMC • Manage Investigational Product inventory levels at depots and clinical sites • Coordinate inventory movement from manufacturers to depots or clinical sites • Design and/or review label text to meet product requirements and regulatory compliance • Manage Investigational Product in accordance with study timing, clinical protocols, cGMP, GCP, ICH, FDA, and applicable regulations • Collaborate with Clinical Operations, CMC, Regulatory Affairs, QA, PDM, external partners, and CMOs • Manage clinical supply and logistics and resolve shipment delays, temperature excursions, and import/export issues • Manage clinical trial contracts, purchase orders, invoices, and clinical supply vendor budgets • Participate in Clinical Supply Chain budget and forecast planning • Represent Clinical Supply Chain at clinical trial meetings • Communicate plans and timelines to internal and external customers and partners

🎯 Requirements

• BS/BA degree in life sciences or business, or equivalent required • Master’s degree in life sciences or business preferred • Minimum 5–7 years of life sciences industry-related experience, including project management, pharmaceutical development, clinical supply management, and/or clinical trials coordination • At least 3+ years in Clinical Supplies Management • Proficient knowledge of Microsoft Excel, PowerPoint, and Project software • APICS certification (CPIM, CLTD, CSCP) preferred • Solid understanding of clinical study design, including randomized, blinded, and open-label studies, and study execution • Knowledge of cGMP, GCP, ICH, FDA, and applicable international, federal, and local regulations