Remote Associate Director, Global Clinical Supply Chain

IMVT Corporation; United States; Remote; USD 170,000 - 200,000; Full time

Benefits offered by this job

Medical, dental, vision

401k

Unlimited paid time off

Parental leave

Equity may be provided

Job summary

Immunovant, Inc. is seeking an Associate Director, Global Clinical Supply Chain to lead end-to-end supply management for clinical trials.

You will coordinate with CMC, regulatory, and external partners to ensure uninterrupted IMP supply, schedule manufacturing, packaging, labeling, and distribution globally. The role requires 5+ years in pharma/biotech supply chain, strong project management, and hands-on experience with CDMOs/CROs, IRT systems, and global logistics.

Qualifications

• Bachelor's degree in science, engineering, or another relevant field; advanced degree preferred.
• Five-plus years of pharmaceutical/biotech experience.
• Experience with global pharma development and manufacturing operations for development-stage biologics.

Responsibilities

• Managing and delivering overall project execution across CMC, Supply Chain, Regulatory, and Clinical Development.
• Recommend packaging design, distribution, and blinding strategies; plan initial supplies and resupplies.
• Develop inventory management plans for clinical sites and depots to ensure treatment availability.
• Interpret clinical protocols and create clinical forecasts.
• Oversee study close-out activities including returns reconciliation and destruction processing.
• Manage inventory and shipment logistics of Immunovant products and samples; ensure temperature control.

Skills

Project management

Cross-functional collaboration

Communication

Problem solving

Leadership

Strategic thinking

Education

Bachelor's degree in science or engineering

Advanced degree preferred

Tools

MS Office

Smartsheets

Job description

Immunovant, Inc. is seeking an Associate Director, Global Clinical Supply Chain to lead end-to-end supply management for clinical trials.

You will coordinate with CMC, regulatory, and external partners to ensure uninterrupted IMP supply, schedule manufacturing, packaging, labeling, and distribution globally. The role requires 5+ years in pharma/biotech supply chain, strong project management, and hands-on experience with CDMOs/CROs, IRT systems, and global logistics.