Regulatory Consultant for Biologic Drug Development
4 settimane fa
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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