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Clinical Trial Supply Manager Oxford United Kingdom,  

PSI (company)


Posted on : 05 April 2017

Project Description

Description:
  • Our company is looking for a knowledgeable and experienced Trial Supply Manager to join our Clinical Supplies division. 
  • A person at this position will act as a consultant to organize an efficient supply chain for the company s clinical projects in different locations and liaise with vendors to manage clinical trial products manufacturing and distribution process.
  •  If you have a hands-on, go-the-extra-mile approach and ready to develop the manufacturing and logistical strategy throughout the life-cycle of a clinical study  you may be the person we are looking for!



RESPONSIBILITIES
  • Provide input during the selection of trial supply vendor(s) for company clinical studies 
  • Liaise with company  project teams and external vendors with regard to clinical trial products manufacturing and distribution 
  • Liaison with company  project teams and company divisions with regard to trial supply management 
  • Development of project-specific vendor management plans 
  • Development of project specific manufacturing, packaging and labelling design(s) configurations for clinical trial(s) 
  • Assessment and set-up of clinical trial product distribution schemes, including interactive web tools 
  • Supervision and coordination of manufacturing and distribution services provided by company  vendors 
  • Assessment of project needs in clinical trial products including the development of supply and re-supply plans (strategies) 
  • Interpretation of the Study Protocol and Investigator Brochure 
  • Assessment and coordination of timelines with regard to clinical trial products manufacturing and distribution 
  • Verification manufacturing design and logistic scheme compliance with project requirements and product specifications 
  • Review of vendor documentation related to clinical trial products manufacturing and distribution 



Qualifications
  • Life Sciences degree or Equivalent 
  • Clinical Research experience; 4-5 years of trial supply management experience 
  • Proven experience working with supply chain technologies (i.e. IRT, CTMS, IWRS integration rules and principles) 
  • An in-depth knowledge of GMP, GDP, and GCP principles 
  • Ability to work both independently and in a team environment 
  • Proficiency in standard MS Office applications 
  • Ability to communicate effectively with vendors and internal parties 
  • Strong time management, planning, and organizational skills, result-oriented approach 

Locations

UK OXFORD

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