Associate Director/Director of Clinical Global Supply Chain

Associate Director/Director of Clinical Global Supply Chain

This position will oversee and lead all aspects of Adicet’s global clinical supply chain and logistics. The successful candidate will have a track record of developing and establishing supply chain business processes that support multiple global clinical programs.

Key responsibilities include:

• Responsible and accountable for development and implementation of global processes for demand planning, supply planning, and inventory management


• Responsible for labeling, distribution, monitoring inventory, supply planning, procurement and logistics activities globally across Contract Manufacturing Organizations, management of drug depots for clinical sites for global clinical trials.

• Responsible for oversight of all domestic and international shipments to support TechOps and Clinical Operations


• Provides oversight and management of secondary packaging and labeling operations at CMOs


• Works closely with Technical Operations, Clinical Development, and Clinical Operations teams to understand clinical demand requirements and ensure alignment with study teams to supply plans and timelines


• Collaborate with Regulatory and Manufacturing to ensure labeling is compliant for specific regions


• Represent clinical supply in Clinical Operations study execution team meetings and CMC meetings


• Collaborates with Clinical Operations to create, review, and modify SOPs and key documents for Clinical Trials supply as well as templates for use during clinical trials (request forms, excursion forms, etc.)

• Manage and oversee transport, storage, and distribution operations for global study locations

Qualifications:

• BS with 7+ years clinical supply chain experience in pharmaceutical or biotech industry


• Experience managing CMO, IRT, clinical distribution vendors


• Experience with handling, monitoring, and shipment of cryogenic products required


• Experience with international shipping logistics including generation of pro-forma and commercial invoices


• Understanding of import/export requirements including incoterms and importer of record roles


• IATA training preferred


• Solid understanding of cGMPs, clinical operations, and development processes


• Detailed oriented with ability to work in a fast-changing environment


• Strong analytical, problem solving, and communication skills.


• Strong collaboration and excellent team skills to be successful in cross-functional and multi-cultural teams.

Adicet Bio is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.

At Adicet, our people are our greatest focus. We believe that attracting and retaining the best and brightest is the key to achieving our mission to deliver best-in-class gamma delta T cell therapies for patients fighting cancer.

Adicet is located in a state-of-the-art facility and works to create an incredible office experience with an onsite gym and various other fitness options, abundant, zero-cost, onsite parking with electric vehicle charging stations and free shuttle (Caltrain), company subsidized lunches (delivered onsite daily) and fully stocked breakrooms.

In compliance with California’s pay transparency law and in pursuit of pay equity and fairness, we publish salary ranges for all open positions. The salary of the finalist selected for this role will be set based on a variety of factors, including but not limited to, their qualifications (education, experience, specialty, and training), and peer and market data. This listed salary range represents the Company’s good faith and reasonable estimate of the range of possible compensation at the time of posting.