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Clinical Distribution Manager
Eingestellt von Harvey Nash IT Recruitment Switzerland
Gesuchte Skills: Design
Projektbeschreibung
Harvey Nash is looking for a Clinical Distribution Manager for a 11 + month project in Switzerland.
You are responsible for
. Defining study's IRT user requirement specifications; reviewing and updating IRT supply parameters periodically over study lifetime to ensure availability of clinical supplies based on actual study con-duct, optimize overage and distribution costs
. Generating optimal distribution plans for investigational medicinal products considering aspects such as optimal lot size, costs and overages; triggering and tracking shipments of clinical trial supplies from central depot to regional hubs and loc depots; following up with distribution vendors and local hub/depot contacts, as needed
. Creating and executing an optimal resupply strategy
. Managing shelf life planning on clinical finished good level and extensions of expiry dates and executes against plan to ensure supply continuity
. Forecasting and updating distribution budget; provides distribution cost input for Grant application, requesting PO and ensuring invoices are received and approved on time
. Reviewing clinical trial protocol amendments and providing input to drug supply sections; adapting the packaging design as required to match the amended study design
. Updating the clinical demand plan for a trial and maintaining an accurate clinical demand forecast with appropriate overage based on changes in trial parameters
. Liaising with Clinical Supply Documentation Specialist (CSDS) to amend the label strategy according to changes in study design, study timelines, participating countries and regulatory requirements; creating and driving finalization of CPRs (Clinical Packaging Request) after RIS where required
. Actively participating in CDM Forums activities and meetings, and supporting CDM Forum Lead as required (eg as subject-matter-expert, in process improvement initiatives, etc.)
. Supporting internal/external inspections and audits
. Actively contributing to SOP creation, revisions and updates
Requirements
. a lower degree with work experience
. Project management, stakeholder management, communication
. fluent in English
Are you available immediately, have experience working within a Life Science company? Please send your complete CV (Word documents preferred) to (see below). For further details feel free to call me (see below). I am looking forward to receiving your application.
You are responsible for
. Defining study's IRT user requirement specifications; reviewing and updating IRT supply parameters periodically over study lifetime to ensure availability of clinical supplies based on actual study con-duct, optimize overage and distribution costs
. Generating optimal distribution plans for investigational medicinal products considering aspects such as optimal lot size, costs and overages; triggering and tracking shipments of clinical trial supplies from central depot to regional hubs and loc depots; following up with distribution vendors and local hub/depot contacts, as needed
. Creating and executing an optimal resupply strategy
. Managing shelf life planning on clinical finished good level and extensions of expiry dates and executes against plan to ensure supply continuity
. Forecasting and updating distribution budget; provides distribution cost input for Grant application, requesting PO and ensuring invoices are received and approved on time
. Reviewing clinical trial protocol amendments and providing input to drug supply sections; adapting the packaging design as required to match the amended study design
. Updating the clinical demand plan for a trial and maintaining an accurate clinical demand forecast with appropriate overage based on changes in trial parameters
. Liaising with Clinical Supply Documentation Specialist (CSDS) to amend the label strategy according to changes in study design, study timelines, participating countries and regulatory requirements; creating and driving finalization of CPRs (Clinical Packaging Request) after RIS where required
. Actively participating in CDM Forums activities and meetings, and supporting CDM Forum Lead as required (eg as subject-matter-expert, in process improvement initiatives, etc.)
. Supporting internal/external inspections and audits
. Actively contributing to SOP creation, revisions and updates
Requirements
. a lower degree with work experience
. Project management, stakeholder management, communication
. fluent in English
Are you available immediately, have experience working within a Life Science company? Please send your complete CV (Word documents preferred) to (see below). For further details feel free to call me (see below). I am looking forward to receiving your application.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Medien/Design