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Clinical Trial Supply Manager Oxford United Kingdom,  

Posted on : 05 April 2017

Project Description

PSI is looking for a knowledgeable and experienced Trial Supply Manager to join our Clinical Supplies division. A person at this positon 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 lifecycle 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 PSI clinical studies Liaise with PSI project teams and external vendors with regard to clinical trial products manufacturing and distribution Liaison with PSI 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 PSI 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 Qualificaitons 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   To apply, E-mail your CV and application letter at



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