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Clinical Supply Programme Manager - 12 Months - Belgium
Eingestellt von Amoria Bond Ltd
Gesuchte Skills: Client, Design
Projektbeschreibung
Clinical Supply Programme Manager - 12 Months - Belgium
GXP, Clinical Study, Trial, Research, Supply, Packaging, Manufacture, Project Manager, Clinical Trial manager, Clinical Project manager, Clinical Programme Manager, Supply chain, Communication, Budgets, Team management, risk, Clinical Supply, CSP
Our Biopharma leading client is in urgent need of talented, proactive, senior Clinical Supply Programme Manager with a good mix of supply chain, trial and team management experience.
Experience required
Equivalent education or working experience as well as strong Clinical Supply/CTS relevant experience (in pharmaceutical manufacturing/packaging, clinical trials and/or supply chain).
Specific skills
*Project management
*Supply chain management
*Communication & Stakeholder management
*Influence, negotiation, driving CTS visibility/impact
*Networking, collaboration
*Proactivity
*Knowledge of GxPs is highly advantageous
Responsibilities include:
*Defining and maintaining supply strategy to ensure adequate and sufficient forecasting of drug product for assigned programs. Create and maintain high level supply plan for all upcoming trials in relevant client systems.
*Lead and maintain structured oversight on clinical trials (forecasted and on-going) per compound to ensure no supply chain disruption and adequate budget, providing guidance and support to other CTS functions/Global Distribution & Logistics/QA as needed
*Forecasting and Budgets.
*Define/anticipate/influence/optimize packaging design, lead times, clinical, regulatory and technical aspects of upcoming clinical trials.
*Stakeholder management, be an interface/point of contact and involved with Clinical teams, the Programme Director, CMC and Quality.
*Drive or suggest compound-level improvements/alignment within CTS or with Partners like Technical Leads and Clinical Program Directors
*Ensure availability information (eg formulation types, manufacturing sites, shelf life, clinical and technical challenges)
For immediate consideration, please send CV now!
Amoria Bond operates as an employment agency and employment business. No terminology in this advert is intended to discriminate on the grounds of age or experience, and we confirm that we are happy to accept applications from persons of any age or experience for this role.
GXP, Clinical Study, Trial, Research, Supply, Packaging, Manufacture, Project Manager, Clinical Trial manager, Clinical Project manager, Clinical Programme Manager, Supply chain, Communication, Budgets, Team management, risk, Clinical Supply, CSP
Our Biopharma leading client is in urgent need of talented, proactive, senior Clinical Supply Programme Manager with a good mix of supply chain, trial and team management experience.
Experience required
Equivalent education or working experience as well as strong Clinical Supply/CTS relevant experience (in pharmaceutical manufacturing/packaging, clinical trials and/or supply chain).
Specific skills
*Project management
*Supply chain management
*Communication & Stakeholder management
*Influence, negotiation, driving CTS visibility/impact
*Networking, collaboration
*Proactivity
*Knowledge of GxPs is highly advantageous
Responsibilities include:
*Defining and maintaining supply strategy to ensure adequate and sufficient forecasting of drug product for assigned programs. Create and maintain high level supply plan for all upcoming trials in relevant client systems.
*Lead and maintain structured oversight on clinical trials (forecasted and on-going) per compound to ensure no supply chain disruption and adequate budget, providing guidance and support to other CTS functions/Global Distribution & Logistics/QA as needed
*Forecasting and Budgets.
*Define/anticipate/influence/optimize packaging design, lead times, clinical, regulatory and technical aspects of upcoming clinical trials.
*Stakeholder management, be an interface/point of contact and involved with Clinical teams, the Programme Director, CMC and Quality.
*Drive or suggest compound-level improvements/alignment within CTS or with Partners like Technical Leads and Clinical Program Directors
*Ensure availability information (eg formulation types, manufacturing sites, shelf life, clinical and technical challenges)
For immediate consideration, please send CV now!
Amoria Bond operates as an employment agency and employment business. No terminology in this advert is intended to discriminate on the grounds of age or experience, and we confirm that we are happy to accept applications from persons of any age or experience for this role.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
IT Entwicklung, Medien/Design