For our client, a company in Pharma, we are looking for a Project Manager Clinical Supply Chain based in Breda.
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.
Tasks assigned to this role will include:
- Developandemployprojectmanagementtechniques to designandsetupsupplychainsfor clinical studies.Thisincludes:
- 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 characteristics.
- Ensure storage and shipping capabilities plus sufficient capacity for finished drug product is available within Amgen supply chain network (both internal and external) to support global study footprint.
- Design cost efficient (re)supply model to distribute finished drug product via applying risk analysis and mitigation strategy.
- Ensure efficient and smooth hand-over to clinical demand and inventory planning team
- 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
- Performs other functions as assigned
- Knowledge of clinical supply chain management
- Bachelor's/Master's degree or equivalent in logistics, business administration or life science.
- 5 years / 3 years (with Master) relevant working experience, preferably in the biotechnology or pharmaceutical industry, with an in-depth knowledge of supply chain management and clinical research management principles.
- At minimum 5 / 3 years 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)
- Fluency in English, both verbal and written communication
- Advanced experience in MS Office applications
- Experience in using ERP systems, preferably SAP
- Project Management certification (PMP, IPMA)
What do we offer
- Contract via Kelly Services of 1 year (40 hours per week)
- Start date: ASAP
- An international environment where you can learn a lot in challenging projects
T: 06 26326600
When interested please react through the application process with your English resume.
About Kelly Services
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Regarding this role, Kelly Services acts as the official temporary employment agency. When you decide to apply to this role your personal information will be processed in accordance with Kelly's Privacy Statement
In keeping with the AWGB (Algemene Wet Gelijke Behandeling) Kelly Services welcomes applications from any and all eligible candidates regardless of ethnicity, gender, disability, religion, sexual orientation or age.