Associate Director, Global Clinical Supply Chain

Immunovant

. Manage and execute overall project delivery through coordination of CMC efforts across CMC, Supply Chain, Legal, Procurement, Regulatory, Clinical Development, and Clinical Operations.

Posted 11/10/2026full-timeRemote • North Carolina • United StatesSenior💰 $170,000 - $200,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in clinical supply chain management, including inventory management, logistics, and project delivery for global clinical trials. Proven ability to collaborate across cross-functional teams and manage relationships with suppliers while ensuring compliance with industry standards.

Highest-signal resume keywords

Clinical Supply ManagementProject Management SkillsInventory ManagementPharmaceutical/Biotech Industry ExperienceCommunication Skills

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Inventory ManagementProject ManagementClinical Supply Chain OperationsAnalytical DevelopmentFormulation DevelopmentUpstream/Downstream Process DevelopmentTemperature Excursion ProcessesStudy Closeout ActivitiesPackaging DesignBlinding Strategy

Soft Skills

Problem-SolvingLeadershipDecision-MakingCollaborationEntrepreneurial Spirit

Tools & Technologies

MS OfficeSmartSheetsIRT Inventory Management

Industry Keywords

PharmaceuticalBiotechGlobal Clinical TrialsContract CMO FacilitiesClinical DevelopmentRegulatory Compliance

About the role

Key responsibilities & impact

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

What you’ll need

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

Comp & perks

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