The Company has developed a novel drug delivery system - the TEPI Patch® - which can deliver high doses of a wide range of drugs via the skin.  The technology has generated interest from some of the leading transdermal delivery companies in the world. In addition to licensing our technology we are developing our own products.  The first, an ibuprofen TEPI Patch, is progressing into clinical development and the programmes for the next products are being developed.  

The role:

  • Managing international clinical studies, including
  • CRO & vendor selection and oversight
  • Reviewing study-related documents
  • Updating stakeholders on study progress
  • Checking adherence to the contract, SOPs, protocol and regulations
  • Establishing and maintaining a GCP management system

The requirements:

  • Minimum of 5 years’ experience in clinical development
  • Experience of managing CROs
  • Thorough knowledge of ICH/GCP and clinical trial regulations
  • Able to work in the Company’s offices in Coventry at least 2 days a week
  • Competitive salary 

To apply: Send your CV to by 27 August 2017.  Further informaton about the role can also be requested via this email address. No agencies please.