Global Clinical Supply Lead - Cell Therapy

Merck & Co.

New Jersey

On-site

USD 146,000 - 192,000

Full time

8 days ago
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Benefits offered by this job

Medical insurance
Dental insurance
Vision insurance
401(k) with company match
Parental leave

Job summary

Legend Biotech is seeking a Sr. Manager, Clinical Supply Operations to join our Technical Development team in Somerset, NJ.

You will coordinate investigational product planning, packaging, labeling, distribution, inventory, and QA release across global sites, CROs, and vendors. The role requires strong operational discipline, hands-on supply execution, and collaboration across Clinical Operations, CMC, Quality Assurance, Regulatory, and external partners to maintain compliant supply of clinical

Qualifications

  • Bachelor’s degree or equivalent in related field; 6+ years in clinical supply ops or GMP environment.
  • Experience with global clinical trials and working with sites, CROs, depots, vendors.

Responsibilities

  • Coordinate packaging, labeling, distribution, and destruction for multiple trials.
  • Maintain inventory visibility amid evolving protocols and country requirements.
  • Lead day-to-day clinical drug supply activities to ensure availability of investigational product.
  • Develop and maintain demand forecasts, supply plans, and risk-mitigation actions.
  • Collaborate with Clinical Ops, QA, Regulatory, and vendors to ensure compliant supply.

Skills

Clinical planning
Vendor management
Inventory management
GMP compliance
QT/IR T systems
Cross-functional collaboration
Project ownership

Education

Bachelor's degree in supply chain, life sciences, pharmacy, business
Advanced degree or clinical supply certification (preferred)

Tools

IRT systems
CTMS
eTMF
ERP systems

Job description

Legend Biotech is seeking a Sr. Manager, Clinical Supply Operations to join our Technical Development team in Somerset, NJ.

You will coordinate investigational product planning, packaging, labeling, distribution, inventory, and QA release across global sites, CROs, and vendors. The role requires strong operational discipline, hands-on supply execution, and collaboration across Clinical Operations, CMC, Quality Assurance, Regulatory, and external partners to maintain compliant supply of clinical

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