Clinical Supply planner Brabant Walloon consulting Our partner is looking for a Clinical Supply Planner. This international company is well-known for its pharmaceuticals.
What are your responsibilities? Clinical Supply Planning : You refine the Investigational Medicinal Products (IMP) supply strategy to ensure adequate and sufficient forecasting of IMP.
You drive production plan, distribution plan and IRT settings throughout the study You are responsible for creating the IMP distribution strategy to ensure timely and cost efficient delivery to clinical sites using distribution requirements principles.
You manage IMP demand (forecast) and supply fluctuations in order to ensure timely and effective supply availability throughout trial, while managing the risks and minimizing the supply chain costs You are accountable for mitigating all supply disruptions, such as Out of Drug situations, temperature excursions, recalls, depot closures, etc.
Manages the IRT settings to avoid and mitigate risks. You solve issues along the way, analyzing the context, proposing alternatives and reaching out to stakeholders to seek collaboration with the end goal on meeting customer’s needs.
You order packaging as well as resupplies for IMPs, and track releases. Orders and oversees expiry update re-labeling (shelf-life extensions) You manage inventory, order movements of IMP through the established distribution network.
You manage study supply chain through the use of KPI's, such as forecast accuracy, scrap, inventory, enrolment and dispensing rates, etc You monitor clinical and supply assumptions, as well as actuals, to reevaluate the distribution and supply plan throughout the study You ensure Strategic Development Supply Lead visibility on study supply activities and study supply budget variations for assigned trials.
Proactively identifies risks and escalates issues Project Coordination and stakeholders management You guarantee optimal transfer of information / knowledge from CSSM, enabling an efficient conduct of the study, and ensures all deliverables until the study closure of the project You drive strong partnership with stakeholders (CTS functions, Clinical Team, Global Distribution and Logistics (GDL), QA, IRT vendor), acting as a key contributor in Joint Clinical Study Teams as a liaison for CTS during the study maintenance and closure.
Educates and influences as needed, to ensure incorporation of CTS input into decisions impacting the IMP supply chain You are key contributor for achieving the planned milestones regarding clinical supply activities including packaging, labeling and distribution You support functions study closure activities Lead initiatives and projects to improve supply chain planning across using concepts You foster effectiveness, efficiency and encouraging continuous improvements on business processes and SOPs by supporting or leading changes on those.
Others : You are able to travel domestically or internationally for business reasons. You insure all compliant related topics are performed on time (Trackwise, Training plan, SOP reviews,.
Augmented Analytics : is able to build queries, summarize data and compute standard KPI's, including financial skills (ability to manage study and compound budget) Championing change : tolerates risk and uncertainty, understands the need for and supports the process of change, reacts to changing demands What can you expect ?
Jefferson Wells offers you a permanent contract as consultant with an attractive salary package ... Trackwise, Analytics, Supply Planning, Pharmaceuticals, Coaching, Maintenance, ReactJS, Delivery, Business, APICS CPIM, Management, Supply chain, Budget, Forecasting, Acting, ImPACT, Recalls, Leading Change, Forecasting, CTS, Engineering, Networks, Logistics Supply, Production, KPI, Closures, Packaging, Supply and Demand, Quality assurance, Clinical, Depot Originele vacature is te vinden op StepStone.
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