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Life Sciences Stellen Basel

Clinical Trial Supply Manager (f/m), 100%

Einritt: Immediately
Region: Basel
Stelle: Life Sciences
Art: Temporärstelle

Exciting position within a multinational company!


Our customer, a pharmaceutical company based in Basel, needs reinforcement. For a temporary employment (DURATION: 12 MONTHS) we are looking for a

Clinical Trial Supply Manager (m/f), 100%


  • Represents GCS as a core member in the integrated Clinical Trial Team (iCTT); defines and advises the iCTT on the optimal clinical trial supply strategy in terms of, but not limited to, packaging design, technical and timeline feasibility, efficiency and risk management.
  • Reviews overall clinical trial protocol/protocol amendments, provides inputs to develop optimal packaging design, clinical trial supply design and visit schedule.
  • Creates and maintains complete and accurate clinical supply demand for assigned study in alignment with protocol requirements, key study parameters and milestones, patient projections, with appropriate overage and by using defined processes and systems.
  • Creates and drives finalization of the packaging design (Clinical Packaging Request) and a comprehensive label strategy for all participating countries in the clinical trial.
  • Defines clinical supply parameters for NIRT set up and initiates subsequent updates throughout the duration of the clinical trial
  • Develops and executes a trial-level project plan together with all other relevant roles.
  • Identifies, assesses and proactively communicates supply risks to all relevant stakeholders along with appropriate mitigation strategies to ensure supply continuity
  • Collaborates with all relevant line function partners for country submission and approval timelines (including IND-IMPD amendment) to develop optimal supply strategy.


  • Degree in science, engineering or equivalent.
  • Fluent in English
  • At least 5 years of practical experience in chemical / pharmaceutical Industry, 3 years of experience in field of expertise
  • Good expertise in related field
  • Good knowledge about the Drug Development process
  • Basic project management , good organization and planning skills
  • Knowledge of relevant regulations (e.g. GMP, HSE etc.)
  • Demonstrates problem-solving and idea generation skills
  • Good presentation skills
  • Fundamental Leadership skills
  • Very good communication, negotiation and interpersonal skills
  • Ability to work in interdisciplinary teams


Don’t hesitate to call Renato Imboden at 061 269 90 60

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