Associate Director, Global Clinical Supply Chain

🔥 2 minutes ago

🌲 North Carolina – Remote

🌲 North Carolina – Remote

💵 $170k - $200k / year

⏰ Full Time

🟠 Senior

🔗 Supply Chain

👻 Ghost score 5%

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Immunovant

WebsiteLinkedInAll Job Openings

51 - 200 employees

Founded 2018

🏥 Healthcare

🧬 Biotechnology

💊 Pharmaceuticals

Healthcare • Biotechnology • Pharmaceuticals

Immunovant is a company focused on advancing treatments for autoimmune diseases through a patient-focused approach. With a vision of enabling normal lives for people with autoimmune diseases, Immunovant applies its expertise in science to develop and test new therapies. The company emphasizes complex and variable needs across different stages and severities of diseases. Immunovant is committed to pushing forward its therapeutic areas and clinical trials, while also engaging with patients, caregivers, and investors about their ongoing studies and corporate initiatives.

📋 Description

• Manage and execute overall project delivery through coordination of CMC efforts across CMC, Supply Chain, Legal, Procurement, Regulatory, Clinical Development, and Clinical Operations. • Provide recommendations on packaging design, distribution, and blinding strategy. • Plan and manage initial supplies and resupplies for assigned studies. • Design and implement plans to supply study drug to complex global clinical trials. • Develop and execute inventory management plans for clinical sites and depots. • Interpret clinical synopses and protocols and create clinical forecasts. • Execute supply chain inventory management in partnership with Clinical Operations. • Identify potential supply chain issues, analyze them, and recommend solutions. • Perform study closeout activities, including returned goods reconciliation, inventory destruction processing, and file archiving. • Manage inventory and shipment logistics for Immunovant products and associated samples. • Ensure temperature excursion processes are executed as required. • Liaise with suppliers to manage relationships, support rapid startup, resolve issues, and respond to CMC project questions. • Review and adjust IRT strategy and settings to optimize supply chain operations. • Leverage IRT inventory management capabilities to manage studies. • Perform all necessary tasks to ensure effective clinical supply chain operations for assigned trials.

🎯 Requirements

• Bachelor's degree in science, engineering, or another relevant field; advanced degree preferred. • Five-plus years of relevant pharmaceutical/biotech industry experience. • Experience with global pharmaceutical/biotech development and manufacturing operations for development-stage biologics, including upstream/downstream process development, formulation development (pre-filled syringe), analytical development, and device development. • Experience managing diverse project activities with contract CMO facilities at different global locations. • Experience with clinical supply management. • Outstanding project management skills; proven ability to work independently, prioritize, and manage multiple tasks simultaneously. • Strong computer skills including MS Office and SmartSheets. • Hands-on, roll-up-your-sleeves approach with high sense of urgency and drive for results. • Demonstrated communication, problem-solving, leadership, and decision-making skills. • Ability to think outside of the box and challenge the status quo. • Natural entrepreneurial spirit with unrelenting dedication to delivering results. • Desire to work in a fast-paced, innovative environment. • Natural collaborator who enjoys working on a cross-functional team.

🏖️ Benefits

• Equity and other forms of compensation may be provided as part of a total compensation package • Medical benefits • Dental benefits • Vision benefits • 401k • Unlimited paid time off • Parental leave • Flexible Work Environment

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