Undertake activities to assess, plan and set up trial supply schemes for assigned projects
Manage vendors involved in clinical supplies and interactive response technology
Analyse clinical trial protocols and translate requirements to establish an efficient supply chain solution for PSI studies
Build and maintain a drug demand forecast in line with planned enrolments
Plan the optimal campaign strategy, to ensure clinical supplies are available in accordance with the project requirements
Manage the CMO vendor
oversee packaging, labelling, procurement, distribution and QP release activities to ensure supplies are delivered on time
Manage the IRT vendor
lead study specific system set-up, UAT, system acceptance and ongoing system updates
Develop clinical supply plans and provide input for the development of vendor management plans
Participate in the selection of trial supply vendors and IRT vendors for PSI studies
Support and train PSI teams in clinical supply management
Liaise with PSI project teams, company divisions, clients and vendors
Assess risks associated with clinical product management and quality incidences reported by vendors
Support business development tasks related to clinical trial supply services

College or University degree
3-5 years experience in Clinical Supply Chain Management (Essential)
Experience working with supply chain technologies (i.e. IRT, CTMS, IWRS integration rules and principles)
Training in GMP and GDP
Ability to communicate effectively with vendors and internal parties
Ability to work both independently and in a team environment
PC skills to be able to work with MS Word, Excel and PowerPoint

Clinical Supply Chain Manager

Key skills