Associate Director, Clinical Supply Chain

Scorpion Therapeutics; Boston (MA); On-site; USD 180,000 - 240,000; Full time

Job summary

Centessa Pharmaceuticals is seeking an Associate Director, Clinical Supply Chain to lead strategies for delivering Investigational Product across multiple clinical programs. Based in the US, the role coordinates packaging, labeling, logistics, inventory, and demand planning to ensure seamless trial execution.

You will build relationships with internal teams and external CDMOs, drive regulatory documentation and audits, monitor budgets, and mitigate risks, leveraging deep GMP/GDP know-how and

Qualifications

• 7+ years in biotech/pharma clinical supply
• Experience with international programs and CDMOs
• Deep GMP/GDP knowledge and regulatory awareness

Responsibilities

• Build supply strategies for Investigational Product across multiple programs
• Manage relationships with internal teams and external CDMOs
• Develop demand forecasts and oversee packaging, labeling, logistics, and inventory
• Ensure regulatory compliance and support audits
• Oversee budget, risk mitigation, and regulatory documentation

Skills

Clinical supply chain

GMP/GDP knowledge

CDMO management

International experience

Education

Bachelor's degree in engineering or science

Job description

Role:

Associate Director, Clinical Supply Chain at Centessa Pharmaceuticals, focused on developing and executing strategies for delivering Investigational Product across multiple clinical programs.

Responsibilities

Responsibilities include building supply strategies, managing relationships with internal teams and external CDMOs, developing demand forecasts, overseeing packaging, labeling, logistics, and inventory management, and ensuring regulatory compliance. The role involves risk mitigation, budget oversight, and collaboration on regulatory documentation and audits.

Qualifications

Bachelor's in engineering or science; 7+ years in biotech/pharma clinical supply, with international experience and deep GMP/GDP knowledge; proven experience managing CDMOs and supply chain operations.

High-Value

focus on late-phase clinical trials, international logistics, GMP compliance, cross-functional collaboration, and regulatory documentation.

WorkSetup

based in the US with up to 20% domestic and international travel.