Associate Director, Global Clinical Supply Chain - Flexible

Remote Genie; North Carolina; Hybrid; USD 170,000 - 200,000; Full time

Benefits offered by this job

Equity

Medical benefits

Dental benefits

Vision benefits

401k

Unlimited PTO

Parental leave

Job summary

Immunovant, Inc. seeks an Associate Director, Global Clinical Supply Chain to lead end‑to‑end supply chain activities for clinical trials.

You will coordinate with CMC, Regulatory, Clinical Operations, and external partners to ensure uninterrupted IMP supply and timely study starts. The role requires strong project management, collaboration across global teams, and hands‑on oversight of packaging, labeling, distribution, and IRT settings.

Qualifications

• 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.

Responsibilities

• Managing and executing overall Project Delivery through coordination of CMC efforts assigned to the entire project team (including but not limited to CMC, Supply Chain, Legal, Procurement, Regulatory, Clinical Development, and Clinical Operations).
• Provides recommendations on packaging design, distribution and blinding strategy. Plans and manages execution of initial supplies and resupplies for assigned studies.
• Develops and executes inventory management plans for clinical sites and depots to ensure treatment availability for every patient visit.
• Interprets clinical synopsis and protocols and creates clinical forecast.
• Executes supply chain inventory management in partnership with Clinical Operations.
• Proactively identifies potential supply chain issues, provides analysis and recommends solutions.
• Performs study close out activities including returned goods reconciliation, inventory destruction processing, and file archiving.
• Manage the inventory and shipment logistics of all Immunovant products and associated samples. Ensures temperature excursion process is executed as required.
• Liaison with Suppliers to manage relationships and drive triage level activities that require diligent focus with rapid start-up, resolution to issues, and respond to questions related to CMC projects.
• Reviews IRT strategy to ensure it supports the strategic supply plans and ensures that IRT settings are adjusted to optimize the supply chain.
• Leverages the inventory management capabilities of the IRT to appropriately manage studies.
• Perform all necessary tasks to ensure clinical supply chain for assigned trials operates effectively.

Skills

Project management

Cross-functional collaboration

Regulatory knowledge

Clinical supply management

CMO coordination

MS Office

SmartSheets

Communication

Problem-solving

Leadership

Education

Bachelor’s degree in science/engineering or related field

Advanced degree preferred

Tools

MS Office

SmartSheets

Job description

Immunovant, Inc. seeks an Associate Director, Global Clinical Supply Chain to lead end‑to‑end supply chain activities for clinical trials.

You will coordinate with CMC, Regulatory, Clinical Operations, and external partners to ensure uninterrupted IMP supply and timely study starts. The role requires strong project management, collaboration across global teams, and hands‑on oversight of packaging, labeling, distribution, and IRT settings.