Clinical Supply Chain Specialist
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
In this role you will work within the clinical supply chain team in order to lead global design and set up of clinical supply chains. These have to be timely, efficient, effective and independent programs from the first subject enrolment on per country/cluster. These supply chains are developed by project management techniques.
RESPONSIBILITIES
- Create Project Plan to ensure timely clinical study start to support first subject enrolled per country
- Create a study forecast for finished drug product introductions within the applicable systems.
- Design model for cost efficiency of the finished product taking into account mitigation strategy and risk analysis.
- 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 .
- Ensure storage and shipping capabilities and capacity for finished drug product (both internal and external) to support global study footprint.
REQUIREMENTS
Minimum requirement:
- 5 years’ experience within supply and demand planning
- Experience within a highly regulated industry (Pharmaceuticals, biotechnology, medical devices)
- Bachelor or Master in a related field (preferably logistics)
- Knowledge of clinical supply chain management and clinical research management principles.
- General understanding of regulatory guidelines impacting clinical supplies (i.e. GxP, ICH guidelines, Clinical Trial Directive)
- Fluent in English
Preferred Requirements:
- Advanced experience in MS Office applications
- Experience in using ERP systems, preferably SAP
- Project Management certification (PMP, IPMA)
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Pascha Groot.
