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
