Associate Director, Clinical Supply Chain

Scorpion Therapeutics; Cambridge (MA); On-site; USD 150,000 - 230,000; Full time

Job summary

Olema Oncology is seeking an Associate Director, Clinical Supply Chain to lead the planning, development, and optimization of the global clinical supply chain for late‑stage oncology trials, ensuring uninterrupted drug supply.

You will manage inventories, shipping, third‑party manufacturing, packaging, labeling, distribution, and risk mitigation, develop IRT systems, and partner with Clinical Operations to align supply with study demands.

Qualifications

• Bachelor's degree required; Master's preferred.
• 8+ years in biotech/pharma clinical supply chain with GMP, inventory control, global shipping, and late-phase oncology trials.
• Experience with large, late-stage studies in oncology with small molecules.

Responsibilities

• Managing inventories, shipping, third-party manufacturing, and logistics.
• Developing IRT systems.
• Overseeing packaging, labeling, distribution, and risk mitigation.
• Partnering with Clinical Operations to align supply with study demands.

Skills

Communication

Analytical thinking

Project management

Entrepreneurial mindset

Education

Bachelor's degree

Master's degree preferred

Tools

IRT systems

Global shipping

GMP compliance

Job description

Role

Associate Director, Clinical Supply Chain at Olema Oncology, responsible for planning, developing, and optimizing the global clinical supply chain to ensure uninterrupted drug supply for late-stage oncology trials.

Responsibilities

• Managing inventories, shipping, third-party manufacturing, and logistics.
• Developing IRT systems.
• Overseeing packaging, labeling, distribution, and risk mitigation.
• Partnering with Clinical Operations to align supply with study demands.

Qualifications

• Bachelor's degree required, Master's preferred.
• 8+ years in biotech/pharma clinical supply chain management, with expertise in GMP, inventory control, global shipping, and late-phase trials, particularly in oncology with small molecules.

Attributes

• Strong communication, analytical and problem-solving skills, project management proficiency, entrepreneurial mindset, and high ethical standards.

High-Value

• Oncology
• Late-stage clinical development
• Global logistics
• IRT development
• GMP compliance
• Experience with large, late-stage studies

Location

San Francisco or Cambridge, with approximately 15% travel.