Clinical Trial Supply Manager

argenx

Gent, Belgium
Competitive salary pyckage; extensive benefits; no...
Not specified
Master's degree in scientific discipline
Minimum 4 years clinical trial supply experience
Knowledge of gxp regulatory requirements
argenx is seeking a Clinical Trial Supply Manager in Gent, Belgium, to drive clinical trial supply strategies and ensure effective product supply for their expanding pipeline of autoimmune medicines. The role requires collaboration with various stakeholders and a strong understanding of GxP regulatory requirements

Job Summary

  • The role involves driving the development of tailored clinical trial supply strategies aligned with protocols and GxP requirements.
  • Candidates will manage external vendors, coordinate IMP packaging runs, and ensure availability of investigational medicinal products for patients.
  • The position offers a competitive salary package and the opportunity to contribute to a dynamic, human-sized biotech company.

Matching Summary

Match Score: 85

argenx is seeking a Clinical Trial Supply Manager in Gent, Belgium, to drive clinical trial supply strategies and ensure effective product supply for their expanding pipeline of autoimmune medicines. The role requires collaboration with various stakeholders and a strong understanding of GxP regulatory requirements.

Salary

Competitive salary package; Extensive benefits; Not specified

Skills & Requirements

Must-have

  • Master's degree in scientific discipline
  • Minimum 4 years clinical trial supply experience
  • Knowledge of GxP regulatory requirements
  • Experience managing external vendors and distributors
  • Proficiency with IRT systems and drug inventory tracking

Nice-to-have

  • Excellent organization and planning skills
  • Strong communication and stakeholder relationship building
  • Analytical mindset with delivery-oriented focus
  • Flexible attitude with proactive problem solving
  • Working knowledge of MS Office package

Key Requirements

  • Master's degree in scientific discipline or equivalent
  • Minimum 4 years experience in clinical trial supplies
  • Fluent in English

Work Rights

Not specified

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