Job Description


Investigational Product Supply (IPS) Materials Coordinator

Our established Client based in Kent is currently looking for an Investigational Product Supply (IPS) Materials Coordinator to join their Clinical Trial Supply team.
As the Investigational Product Supply Materials Coordinator you will be tasked with co-ordinating Clinical Trial label/packaging activities and ensuring all Clinical Trial Supply packaging specifications/documentation are created within deadlines set by our Client and within cGxP guidelines.
Key Responsibilities as the Investigational Product Supply Coordinator
* Follow batch documentation for labelling and packaging activities in line with cGMP
* Store and maintains IMP within specified storage conditions
* Manage inventory of packaging components
* Keep accurate records of IMP and components
* Coordinate the return of IMP from clinical sites
* Organise waste for destruction, ensuring accurate records are maintained to facilitate end of study reconciliation
* Provides input into the quality management system as required
Skills / Attributes:
* A good standard of education including excellent numeracy and literacy skills
* A working knowledge of cGMP would be advantageous
* Excellent attention to detail
* Able to follow instructions e.g. batch documentation and Standard Operating Procedures (SOPs)
* Working knowledge of Microsoft Office (Outlook, Word, Excel)
* High level of Good Manufacturing Practice according to MRHA and FDA Guidelines - desirable
* Recent and relevant experience of working within a Pharmaceutical environment - desirable
* Previous experience in or exposure to IXRS is desirable but not essential
If you feel your experience matches our Clients requirement for an Investigational Product Supply (IPS) Coordinator please forward your c.v. TODAY