Clinical Supply Chain Associate

SIRE LIFE SCIENCES; Breda; On-site; EUR 48,000 - 64,000; Full time

Job summary

A leading life sciences company in Breda is seeking a Clinical Supply Chain Associate to coordinate the design and maintenance of supply chains for clinical studies. Responsibilities include managing SAP master data, coordinating artwork, and ensuring availability of study materials for global clinical programs. The ideal candidate has a bachelor's degree in Supply Chain or a related field and experience in the pharma/biotech industry. Join this exciting full-time role for an opportunity to support global clinical trials effectively.

Qualifications

• Bachelor’s degree in Supply Chain, Logistics, Life Sciences, or a related field.
• Experience in pharma/biotech or clinical logistics.
• Understanding of GMP/GDP/GDocP standards and SAP systems.

Responsibilities

• Manage SAP master data and ensure timely material availability.
• Coordinate artwork and labeling processes.
• Support setup of study design tables and depot plans.
• Maintain documentation for global clinical supply operations.
• Collaborate with cross-functional teams for compliance and efficiency.

Skills

Planning and coordination

Knowledge of GMP/GDP/GDocP

Experience in pharma/biotech

Education

Bachelor’s in Supply Chain or related field

Tools

SAP systems

Job description

About the Role

As a Clinical Supply Chain Associate, you’ll coordinate the design, setup, and maintenance of supply chains for clinical studies in a GMP/GDP-regulated environment. You’ll manage SAP master data, coordinate artwork creation, and ensure all study materials are available on time for clinical programs worldwide.

Key Responsibilities

• Manage SAP master data and ensure timely material availability
• Coordinate artwork and labeling processes
• Support setup of study design tables and depot plans
• Maintain documentation and reporting for global clinical supply operations
• Collaborate with cross-functional teams to ensure compliance and efficiency

Qualifications & Requirements

• Bachelor’s in Supply Chain, Logistics, Life Sciences, or related field
• Experience in pharma/biotech or clinical logistics
• Knowledge of GMP/GDP/GDocP and SAP systems
• Strong planning and coordination skills

Other Information

This full-time position in Breda offers an exciting opportunity to work in an international environment where your expertise directly supports global clinical trials.

Looking forward to speaking with you!