jobid=A.0.0672
Sr. Associate Global Study Planner
Location: Amgen Breda, The Netherlands
As a Sr. Associate Global Study Planner, you play a key role in planning and coordinating clinical drug studies on a global scale. You’ll work in an innovative, international environment where science, collaboration, and impact are central.
Your Responsibilities
As a Global Study Planner, you are responsible for demand and supply planning for clinical studies (typically fewer than 10). You ensure timely and efficient availability of drug products from study start to last patient dosed. You’ll collaborate closely with colleagues in the UK and US and be involved in:
- Forecasting and inventory management of clinical drug supplies
- Coordinating packaging, labeling, and shipment
- Managing risks and resolving logistical challenges
- Participating in improvement initiatives and cross-functional meetings
- Using systems such as SAP, forecasting tools, dashboards, and internal documentation
What You Bring
- Bachelor’s degree in logistics, business administration, or equivalent
- Minimum of 5 years’ experience in supply planning, preferably in the pharmaceutical industry
- Fluent in English (spoken and written)
- Experience with ERP systems (preferably SAP) and MS Office
- Knowledge of clinical supply chain processes and GMP guidelines
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