sr. associate global study planner.

• Salary of € 3.917 - € 4353 gross per month
• Breda, you have to be available to work on site
• Job for 40 hours per week
• International pharmaceutical company

who are you

Knowledge of supply chain management and minimum of 5 years relevant working experience is necessary to be successful in this position.

What do you bring?

• Bachelor’s degree in logistics, supply chain or business administration
• Knowledge of (clinical) supply chain management
• Minimum 5 years relevant working experience in supply planning, preferably in the pharmaceutical industry
• Fluency in English, both verbal and written communication
• Preferred Requirements: Advanced experience in MS Office applications, Experience in using ERP systems, preferably SAP, Basic understanding of regulatory guidelines impacting clinical supplies

what will you do

In this role you independently execute Demand and Supply Planning processes for dedicated clinical studies with a global scope. You ensure Finished Drug Product supplies from study start throughout last patient dosed and you are involved until study closure. It is your responsibility to coordinate efficient and effective operational inventory management. Balance ensure supplies and minimizing scrap during the full length of the study.

The global study planner is responsible for the demand and supply planning for the assigned clinical studies, typically less than 10 studies by planner. You manage the packaging and labeling orders to ensure supply based on the latest expected demand for a study. You ensure supply readiness for each new study that is about to start. You represent the planning steam in improvement initiatives and cross functional meetings. You manage performance through daily SQDIP Performance Board and adhere to the targets for supply and demand driven metrics and measures.

• You are involved and prepared for forecasting drug conversations and adjust system settings timely to reflect the latest expectations on study demand until end of trial. This includes attending and leading meetings with the study manager based in UK
• Based on demand at the clinical sites and available supplies that hit an expiry date, you ensure supply in the central warehouses and all sites that participate in the clinical trial. Indicate ratio, volume and timing of packaging and shipment of pac
• You balance the right amount of inventory with the scrap risk and management guidance on inventory levels.
• You resolve logistical conflicts impacting studies and R&D milestones ensuring that supplies are not on the critical path
• You promptly identify and escalate risks to study timelines or clinical supplies, from a supply chain perspective, to all key stakeholders and internal management
• You utilize systems to effectively manage key product such as the Forecasting system, SAP, Hospital inventory and dosing system, Dashboard controls and internal documents as a source for daily activities.
• You articulate clearly the clinical supply chain management processes and strategies to key stakeholders
• You negotiate resolution of resource conflicts where necessary and actively participate in planning meetings to ensure that project needs, priorities, and timing are understood.

where will you work

Your new employer is an American organization which specializes in biotechnological medicines, with a powerful sense of a shared purpose towards its mission: 'To Serve Patients'. The company receives its products as semi-manufactured goods, which are then packed country-specific, stored and eventually shipped to various countries worldwide.

What else can you expect?

• A challenging job at an international company. A gross monthly salary between € 3.466 - € 3.865 gross per month based on a 40 hour working week, salary depends on experience. Also you will receive a travel allowance of €0.29 per km.
• In addition to your salary, you have 30 vacation days per year and 8,33% holiday allowance;
• You will receive your salary every week as we handle a weekly payment.

job application

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