Strategic Lead - Clinical Supply Chain & Operations

Isomorphic Labs; Cambridge (MA); Híbrido; USD 140 000 - 200 000; Tempo integral

Resumo da oferta

Isomorphic Labs is pursuing frontier AI to accelerate drug discovery and transform medicine. We seek a proactive Clinical Supply Chain lead to design end‑to‑end CTM planning, vendor management, packaging, labeling, inventory, and global distribution within an AI‑first team.

You will partner with Clinical Operations, QA, and Regulatory to ensure uninterrupted supply and compliant manufacturing, while building scalable processes for future trials and modalities.

Qualificações

• 7+ years of direct experience in clinical supply chain management, clinical logistics, or investigational material management.
• Experience supporting clinical trials with logistics, replenishment, and flexible kit demand.
• Knowledge of cGMP, GDP, ICH, and regulatory requirements.
• Strong communication and cross‑functional leadership skills.

Responsabilidades

• Clinical Supply Planning & Execution: forecast demand, ensure dosing continuity, minimize waste.
• Packaging, labeling & distribution logistics: manage depots, shipping, and regulatory compliance.
• CRO/IRT/RTSM collaboration: align supply readiness with timelines and regulatory approvals.
• Supply chain scalability: drive software, inventory tracking, and dashboards as development scales.
• Quality, compliance & vendor governance: manage RFPs/SOWs, KPIs, and auditing readiness.

Conhecimentos

Clinical supply chain

Vendor management

Forecasting

Regulatory compliance

Cross-functional leadership

Formação académica

Bachelor’s or Master’s degree in Supply Chain or Life Sciences

Descrição da oferta de emprego

Isomorphic Labs is pursuing frontier AI to accelerate drug discovery and transform medicine. We seek a proactive Clinical Supply Chain lead to design end‑to‑end CTM planning, vendor management, packaging, labeling, inventory, and global distribution within an AI‑first team.

You will partner with Clinical Operations, QA, and Regulatory to ensure uninterrupted supply and compliant manufacturing, while building scalable processes for future trials and modalities.