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Clinical Studies Logistics Manager

Job Description
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