Remote Clinical Supply Chain Manager for IP Trials

Socket.dev; Boston (MA); On-site; USD 105,000 - 150,000; Full time

Benefits offered by this job

401(k) plan

Medical insurance

Dental insurance

Vision insurance

Life insurance

Paid time off

Health and wellness program

Job summary

Centessa Pharmaceuticals is seeking a Manager, Clinical Supply Chain to lead end-to-end planning, execution, and maintenance of uninterrupted clinical supply for IP, comparators, and materials. You will ensure GMP/GDP compliance, timelines, and budgets while partnering across Clinical Operations, CMC, QA, Regulatory, Finance, and vendors.

The role involves managing forecasts, IRT usage, labeling, packaging, and global distribution, with remote work in the US and up to 20% travel.

Qualifications

• Bachelor's degree in engineering or science required.
• 3–5 years biotech/pharma experience in clinical supply chain, including international experience.
• Knowledge of GMP/GDP requirements.
• Experience coordinating cross-functional project teams and external vendors.
• Ability to work independently in a fast-paced environment.

Responsibilities

• Contribute to development and execution of clinical supply strategies for early- to mid-phase trials.
• Manage clinical supply plans, demand forecasts, and inventory strategies including IRT systems.
• Support packaging, labeling, distribution, and resupply of IP and comparators.
• Ensure on-time delivery of clinical supplies to depots and sites globally.
• Partner with Quality, Clinical, CMC, and external CDMOs on labels and schedules.
• Coordinate with external vendors for shipping and licenses.

Skills

Organizational skills

Analytical skills

Decision making

Interpersonal skills

Attention to detail

Education

Bachelor's degree in engineering or science

Job description

Centessa Pharmaceuticals is seeking a Manager, Clinical Supply Chain to lead end-to-end planning, execution, and maintenance of uninterrupted clinical supply for IP, comparators, and materials. You will ensure GMP/GDP compliance, timelines, and budgets while partnering across Clinical Operations, CMC, QA, Regulatory, Finance, and vendors.

The role involves managing forecasts, IRT usage, labeling, packaging, and global distribution, with remote work in the US and up to 20% travel.