Clinical studies logistics manager

Job Description

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For the R&D site of an international company in Utrecht, we are looking for a Clinical Studies Logistics Manager. In this role, you will be responsible for the entire logistics process of clinical study supplies: from planning and labeling to distribution and returns. You will work within a multidisciplinary clinical research team and contribute to the success of medical and early life nutrition studies.

Responsibilities

• Manage study supplies within planning, budget, and in compliance with GCP, GMP, GDP, and applicable regulations
• Translate study protocols into a supply strategy and demand forecast
• Coordinate production and release processes with internal departments and external suppliers
• Organize blinding, randomization, and digital support systems
• Prepare labels in accordance with applicable regulations
• Order and ship lab kits and study-specific materials
• Manage external partners such as warehouses and IT suppliersIdentify and implement quality improvements and draft SOPs

Profile

• Bachelor's or Master's degree in Life Sciences or a related field
• Experience in (international) clinical study management with a focus on logistics and study products
• Knowledge of ICH-GCP, GMP, and GDP
• Proactive, stress-resistant, and well-organized
• Quality-driven and efficient
• Strong communication skills
• Team player who can also work independently

Terms of Employment

• Contract type: Temporary assignment / Secondment
• Duration: 12 months
• Salary: 5000-7000
• Hours: 32 hours per week
• Language: English
• Location: Utrecht

Vacancynumber: 26376