Remote Clinical Supply Chain Leader

Sumitomo Pharma; Santa Fe (NM); Remote; USD 131,000 - 164,000; Full time

Job summary

Sumitomo Pharma America, Inc. is seeking a Clinical Supplies Manager to lead end-to-end supply chain activities for clinical programs.

The role ensures timely Investigational Product availability, manages packaging and labeling, and coordinates with CMOs and vendors to align with study timelines. The position requires 5–7 years in life sciences with clinical supply experience, strong project management, and knowledge of cGMP and regulatory standards.

Qualifications

• BS/BA in life sciences, business, supply chain, pharmaceutical sciences or related field.
• Equivalent combination of education, training, and relevant experience may be considered.
• Minimum 5–7 years in life sciences with project management and clinical supply experience.
• 3+ years in Clinical Supplies Management.
• Experience managing clinical trial materials and vendor coordination.

Responsibilities

• Lead end-to-end Clinical Supply Chain activities for early- and late-phase programs.
• Develop and maintain clinical supply forecasts and timelines in collaboration with stakeholders.
• Translate protocol requirements into practical supply strategies.
• Identify and manage supply risks and issues across manufacturing, packaging, and distribution.

Skills

Project management

Clinical supply management

Pharmaceutical development

Clinical trials coordination

Vendor coordination

Education

BS/BA in life sciences, business, or related field

Master's degree preferred

Tools

IRT/RTSM systems

Excel

PowerPoint

Project

Job description

Sumitomo Pharma America, Inc. is seeking a Clinical Supplies Manager to lead end-to-end supply chain activities for clinical programs.

The role ensures timely Investigational Product availability, manages packaging and labeling, and coordinates with CMOs and vendors to align with study timelines. The position requires 5–7 years in life sciences with clinical supply experience, strong project management, and knowledge of cGMP and regulatory standards.