Clinical Trial Supply Manager

Description du poste

# Clinical Trial Supply Manager # (m/f/d) Freelance/temporary employment for a project Basel Stadt Start date: asap Reference number: 878581/1 ### Responsibilities ### * Study supply leadership to ensure timely planning and execution of supply strategy for continued supply of clinical finished goods (supply drugs) to patients * Develop plans, set up and manage end to end clinical supplies for complex studies in a very diverse portfolio ranging from traditional set up of clinical trials to advanced and innovative set up for Radio Ligand and Cell and Gene Therapy studies * Provide inputs in clinical study protocol, understand study design and are responsible for optimal clinical trial supply strategy in terms of packaging design, pro- active planning following a risk-based approach * Provide patient centric optimal packaging design solutions and optimal packaging and distribution plans for different phases of clinical trials * Independently, and cost efficiently manage IRT, packaging and distribution vendors throughout the study duration including closing activities * Qualitative set up and usage of GMP planning systems (SAP and Rapid Response) to ensure cross functional planning of resources and clinical supplies * Represent Global Clinical Supply as a single point of contact (SPOC) at trial level for the Clinical Trial team (CTT) ### Profile ### * Masters or Doctorate in life sciences (or MBA with bachelor-s degree, or equivalent experience in life science) * Practical experience in clinical supplies within the pharmaceutical industry * Strong operational excellence with high attention to details * Advanced project management, good organization, and planning skills * Broad technical knowledge in appropriate Supply Chain systems used for forecasting and demand planning (solid expertise with SAP) * Data and Digital savviness with high learning agility * Strong background on GMP processes and requirements is desirable ### Benefits ### * A very renowned company * You will work in an international environment