Clinical Trial Supply Manager

Basel-Stadt  ‐ Vor Ort
Dieses Projekt ist archiviert und leider nicht (mehr) aktiv.
Sie finden vakante Projekte hier in unserer Projektbörse.

Beschreibung

We are recruiting for a Clinical Trial Supply Manager who will be responsible for the definition and execution of an optimal clinical trial supply strategy. You will be responsible for the effective risk management to ensure supply continuity to patients. You will lead and manage all projects and participate in cross-functional teams. In return you will have the opportunity of working with a leading Pharmaceutical company which will offer excellent career progression opportunities as well as a great salary package.

Responsibilities:
  • Define the optimal clinical trial supply strategy taking into consideration packaging design, technical and timeline feasibility, efficiency and risk management.
  • Review overall clinical trial protocol and provide inputs to develop optimal packaging design and clinical trial supply design.
  • Create and maintain complete and accurate clinical supply demand for studies.
  • Create and drive finalization of the packaging design and a comprehensive label strategy for all participating countries in the clinical trial.
  • Define clinical supply parameters and initiate subsequent updates throughout the duration of the clinical trial
  • Develop and execute a trial-level project plan together with all other relevant roles.
  • Identify, assess and proactively communicate supply risks to all relevant stakeholders along with appropriate mitigation strategies to ensure supply continuity
  • Collaborate with all relevant line function partners for country submission and approval timelines to develop optimal supply strategy.
  • Generate optimal distribution plans for investigational medicinal products (IMPs), jointly with partner functions.
  • Develop, maintain and execute an optimal resupply strategy with proactive planning, appropriate lead-time and replenishment quantities to ensure compliance and continuity of clinical supplies, including proactive expiry management of clinical supplies.


Requirements:
  • BSc in Science, Engineering or equivalent.
  • 5 years of practical experience
  • Good knowledge about the Drug Development process
  • Project management, good organization and planning skills


Kontakt: Luchele Mendes ()

Michael Bailey International is acting as an Employment Business in relation to this vacancy.
Start
02/2019
Dauer
01/02/2020
Von
Michael Bailey Associates
Eingestellt
16.01.2019
Projekt-ID:
1702399
Vertragsart
Freiberuflich
Um sich auf dieses Projekt zu bewerben müssen Sie sich einloggen.
Registrieren