Clinical Supplies Specialist - Fixed Term

Job type:
Start date:
12 Months
Real Staffing
South East England
Published at:
flag_no United Kingdom
Project ID:

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My client is looking for a Principal Global Clinical Trial Supplies Specialist to join their team providing key support for Global Drug Development compliance, process, and training programs. This leading pharmaceutical company has an envious pipeline and this position has come about due to company growth.

Main responsibilities (to include but not be limited to):
  • Ensure timely and cost efficient supply availability at study start and throughout entire process using all available software systems
  • Represents supply chain function at strategic client group meetings
  • Responsible for administration and maintenance of the Global Development audit
  • Responsible for the collection and review of quality compliance metrics
  • Provides management reports
  • Conducts quality control review of documents and processes
  • Financial responsibilities

  • Educated to Degree level in Science/Life Sciences
  • Significant experience within clinical research
  • Good understanding of GCP ICH guidelines
  • Excellent knowledge of concepts of clinical research and drug development
  • Ability to understand technical, scientific and medical information

This is a fantastic opportunity offering the successful candidate a permanent position within a reputable organisation

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