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Clinical Trial Supply Manager

  • Ubicación:

    Amberes, Bélgica

  • Contacto:

    Aurore Munaut

  • Tipo de trabajo:

    Contract

  • Teléfono de contacto:

    +32 10 68 53 31

  • Industrias:

    Life Sciences, Clinical Research

  • Correo de contacto:

    aurore_munaut@oxfordcorp.com

Our pharma client is looking for a Clinical Trial Supply Manager for a long-term assignment. Do you have this experience and are you looking forward to discover this aspect further in a global pharma environment ? Then this may be a great challenge for you !

Job Description

The Clinical Trial Supply Manager manages clinical supply forecasting, planning, design, execution, and delivery.

Responsibilities

  • Manages clinical supply forecasting, planning, design, execution, and delivery.
  • Tracks department's performance against established metrics.
  • Acts as liaison between department and other relevant groups to establish demand estimates for clinical supplies to meet study requirements.
  • Evaluates, develops, and monitors long-range program and product requirements.
  • Implements new or improved processes, procedures or methodologies.
  • Contributes to the development of departments standard operating procedures.
  • Manages coordination of the clinical supply chain with internal clients and outside contractors.
  • Analyzes and anticipates project problems and obstacles as they relate to clinical supplies and participates in logistics plan adjustments.
  • Oversees the return and destruction of used clinical materials from investigational sites.
  • Establishes and manages the department budgets and controls expenditures within established budgets.
  • Collaborates with other relevant departments to ensure alignment of project activities.
  • Authors the clinical supplies section of project protocols.



Requirements

  • Min. 3 years of experience in Clinical Trial Supplies management for phase I to phase III international clinical studies.
  • Broad understanding and experience in the main tools related to IMP management.
  • Broad understanding of regulatory and Good Manufacturing Practices requirements for IMP supply.
  • Project management skills.
  • Excellent communication skills, ability to work cross-functionally.
  • Fluency in English, Dutch is a plus.
  • Existing right to work in Europe required.

Benefits

  • A balanced salary package based on your capabilities and experience
  • Long-term assignment


Vacancy number: 20932