Regulatory Consultant for Biologic Drug Development

4 settimane fa


Trieste, Friuli Venezia Giulia, Italia ICGEB A tempo pieno
Regulatory Expert for Biologic Drug Development

ICGEB is seeking a qualified expert advisor to work on regulatory requirements for the INTERREG funded research project "PROMOS – Strengthening the bio-medical ecosystem" with partners based in Italy and Austria.

The project aims to map regulatory aspects of biological drug development and its clinical application in Italy and Austria over a 12-month period. The goal is to define a roadmap to bring pre-clinical cell-based therapies to clinical phase research.

Key Responsibilities:

  • Mapping regulatory aspects of biological drug development and its clinical application
  • Defining a roadmap for pre-clinical cell-based therapies
  • Collaborating with partners in Italy and Austria

Requirements:

  • Expertise in regulatory requirements for biologic drug development
  • Experience in clinical application of biological drugs
  • Strong collaboration and communication skills

Please contact us for more information.



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