)
)
Clinical Trial Supply Manager (M/F/D)
Tasks:
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
Qualification:
Masters or Doctorate in life sciences (or MBA with bachelor’s degree, or equivalent experience in life science)
> 5 years of 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 (minimum 3 years of expertise with SAP)
Data & Digital savviness with high learning agility
Strong background on GMP processes and requirements is desirable
Requirements:
Start: 01.07.2026
Duration: 18 months
Capacity: 5 days per week (on-site role)
Location: Basel, Switzerland
)