The Company
A well-known pharmaceutical company committed to enhancing healthcare and enhancing patients' well-being through extensive research and innovative solutions in areas such as oncology, cardiovascular diseases, autoimmune disorders, bone health, and neurology.

Role Description
As a Clinical Supply Chain you will lead the worldwide planning and establishment of clinical supply chains for the designated clinical programs and studies, emphasizing punctuality, efficiency, effectiveness, and autonomy.

Responsibilities
– Use project management methods to create clinical study supply chains.
– Make a project plan to start clinical studies on time for the first subject in each area or storage location.
– Keep track of the expected amount of finished drug product needed for the study in appropriate systems.
– Plan how the finished drug product should be packaged, taking into account the study requirements and the product's characteristics.
– Create a cost-effective way to distribute the finished drug product, considering risks and ways to reduce them.

Requirement
– A bachelor's degree in logistics, business administration, or life science.
– Over 3 years of experience, particularly in the biotechnology or pharmaceutical industry, and knowledge in supply chain management and clinical research management.
– A minimum of 3 years of experience in project leadership and management is required.
– Have a basic understanding of GxP, ICH guidelines, and the Clinical Trial Directive.
– Proficiency in MS Office and experience with ERP systems, especially SAP, is important.

Other Information
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