IPS Coordinator (CTS Department) – 12 Month Contract

South East, UK

The Role

We are currently looking for an Investigational Product Supply (IPS) Coordinator for the Clinical Trial Supply (CTS) department tasked with co-ordinating Clinical Trial label/packaging activities and ensuring all Clinical Trial Supply packaging specifications/documentation are created within deadlines set by the business and within cGxP guidelines.

Key Responsibilities

• Preparation of study specification files.
• Preparation of packaging documentation and labels for all IMP to be used in GW Pharma clinical studies.
• Organising and scheduling of relevant department activities.
• Oversight and co-ordination of IXRS study resupply.
• Maintaining compliance with GW SOPs and creating new/managing existing GW SOPs.
• Creation and maintenance of cGxP documents.
• Planning and management of project tasks.

Essential Skills

• Good working knowledge of Clinical Trial designs.
• Excellent numeracy and literacy skills.
• Excellent planning skills.
• Good communication skills (including written communication).
• Good working knowledge of standard Microsoft packages, i.e. Excel and Word.
• Excellent attention to detail.
• Willingness to work as a team player.
• Ability to use own initiative when working on individual projects.

Desirable

• High level of Good Manufacturing Practice according to MRHA and FDA Guidelines.
• Recent and relevant experience of working within a Pharmaceutical environment.
• Previous experience in or exposure to IXRS is desirable but not essential.

Location: South East, UK

To apply please send your CV with salary expectations to via the apply online button: