Senior Global Clinical Supply Lead

Socket.dev; New Jersey; On-site; USD 146,000 - 192,000; Full time

Benefits offered by this job

Health insurance

401(k) retirement plan

Parental leave

Paid time off

Job summary

Legend Biotech seeks a Sr. Manager- Clinical Supply Operations to join the Technical Development team in Somerset, NJ.

You will oversee hands-on execution of global patient supply activities for early cell and gene therapy programs, coordinating packaging, labeling, distribution, inventory, and releases across sites, CROs, and vendors. Ideal candidates bring 6+ years in clinical supply, strong GMP knowledge, and proven ability to manage multiple studies and vendors while ensuring compliance and

Qualifications

• Bachelor’s degree in supply chain, life sciences, pharmacy, business, or related discipline.
• 6+ years of progressive experience in clinical supply operations or GMP environments.
• Hands-on experience with planning, forecasting, labeling, distribution, reconciliation and destruction.

Responsibilities

• Coordinate global clinical supply activities across studies, sites, and vendors.
• Maintain inventory visibility, forecasts, shelf life, and country requirements.
• Manage temperature excursions, expiry risk, shipment issues, and documentation gaps.
• Lead packaging, labeling, distribution, returns, and destruction aligned with enrollment.
• Ensure inspection-ready documentation and effective use of IRT, ERP, and eTMF systems.

Skills

Clinical supply

GMP & QA

Inventory management

Forecasting

Vendor management

Cross-functional collaboration

IRT familiarity

Project ownership

Education

Bachelor's degree

Advanced degree preferred

Tools

CTMS

eTMF

ERP systems

Vendor portals

Job description

Legend Biotech seeks a Sr. Manager- Clinical Supply Operations to join the Technical Development team in Somerset, NJ.

You will oversee hands-on execution of global patient supply activities for early cell and gene therapy programs, coordinating packaging, labeling, distribution, inventory, and releases across sites, CROs, and vendors. Ideal candidates bring 6+ years in clinical supply, strong GMP knowledge, and proven ability to manage multiple studies and vendors while ensuring compliance and