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Responsible for global Supply Chain activities for Investigational Medicinal Products (IMPs) of national and international Phase I-IV clinical trials in the Therapeutic Area General Medicine
Function as the main point of contact to Clinical Operations and Clinical Development for assigned trials, ensuring the timely and cost efficient provision of clinical supplies
Act as the responsible leader of the CTSU trial team within the matrix structure, ensuring cross-functional collaboration and development of interfaces for all Supply Chain activities on the basis of business, regulatory and industry needs
Provide input to clinical trial protocols and bulk demands incl. comparator and non-IMP commercial products, to specific packaging designs and efficient distribution strategies
Support investigations as Subject Matter Expert for assigned trials
Master's degree in natural sciences or similar disciplines or completed vocational training with experience in clinical trials
Several years experiences in clinical trial supplies or related business
Experience in working in an international environment, as well as team leading and project management experiences
Ideally good knowledge and understanding of the regulatory and GMP/GCP requirements for IMPs
Ability to interpret complex project requirements
Good software skills (MS-Office)
German language skills, written and spoken
Fluency in written and spoken English
Strong problem solving capabilities with the willingness to make decisions and the ability to drive results
Very good communication, negotiation and presentation skills
Ability to work independently as well as in a team
Option of permanent employment with our business partner
Extensive social benefits, incl. Christmas and holiday bonuses
Up to 30 days vacation per year
Free online courses, e.g. several language courses