Project Manager Clinical Supply Chain
Location: BredaProject Manager Clinical Supply Chain
The Company
Or client in Breda is one of the biggest pharmaceutical companies in the world that aims to provide therapies for patients worldwide. Their mission is to deliver innovative medicines for patients worldwide.
Role Description
The Project Manager, Clinical Supply Chain is responsible for leading the global design and set up of end to end customized clinical supply chains in support of the assigned clinical programs/studies in a timely, efficient, effective and independent manner.
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.
- Create and maintain study forecast for finished drug product (both Amgen and non-Amgen) in applicable systems to support clinical study start
- Design optimal packaging configuration for finished drug product taking into account protocol requirements and product.
Requirements
- Knowledge of clinical supply chain management
- Bachelor’s degree or equivalent in logistics, business administration or life science.
- Relevant working experience, preferably in the biotechnology or pharmaceutical industry.
- Experience in project leadership and project management techniques in an international and regulated environment.
- General understanding of regulatory guidelines impacting clinical supplies (i.e. GxP, ICH guidelines, Clinical Trial Directive)
Other information:
Are you ready to take a new step in your career? If you are interested please upload your resume using the apply button.
Requirements
- Knowledge of clinical supply chain management- Bachelor’s degree or equivalent in logistics, business administration or life science.
- Relevant working experience, preferably in the biotechnology or pharmaceutical industry.
- Experience in project leadership and project management techniques in an international and regulated environment.
- General understanding of regulatory guidelines impacting clinical supplies (i.e. GxP, ICH guidelines, Clinical Trial Directive)
Other information:
Are you ready to take a new step in your career? If you are interested please upload your resume using the apply button.
