Supply Chain Specialist Clinical
Location: NetherlandsSIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!
THE COMPANY
Our client is a professional Pharmaceutical organization, based in Noord-Brabant Netherlands.
This company discovers, develops and produces new innovative human therapeutics that improve the life expectancy of humanity.
ROLE DESCRIPTION
For this position you are responsible for the management of clinical supplies during the execution phase of clinical trials consistent with GMP guidelines. Responsible for the management of all clinical supplies during trial execution (large and small molecules and for all phases of clinical trials).
RESPONSIBILITIES
-Develop and employ project management techniques to design and set up supply chains for clinical studies
-Create and maintain project plan to ensure timely clinical study start to support first subject enrolled per country cluster/ depot
-Create and maintain study forecast for finished drug product in applicable systems to support clinical study start
-Design optimal packaging configuration for finished drug product taking into account protocol requirements and product characteristics
-Ensure storage and shipping capabilities plus sufficient capacity for finished drug product is available within the supply chain network (both internal and external) to support global study footprint
-Design cost efficient (re)supply model to distribute finished drug product by taken into account risk analysis and mitigation strategy.
-Facilitate the phase in phase out strategy for new medicinal product introduction, such as running scenario’s, impact on study demand and set up activities for formulation and device introductions
REQUIREMENTS
-Bachelor or Master’s degree
-4-6 years experience preferably in a clinical supply related role
-Experience with clinical supply demand management tools (e.g., tcVisualize, IVRS, SAP)
-General knowledge of GxP principles
-Intermediate to advanced software skills (e.g., Microsoft Excel, Powerpoint)
-Excellent written and verbal communication skills
-Strong planning and cross-functional coordination skills
-Strong attention to detail
-Ability to work independently with some coaching
-Ability to multi-task and manage complexity
-Ability to work in a high pressure environment
-Solution oriented
-Exceptional collaboration skills
-Integrity and Credo Based-actions
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Leon Moonen.
