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Global Clinical Supply Chain Manager - Remote/Uxbridge

Gibbs Hybrid
Posted 11 days ago, valid for 14 days
Location

Uxbridge, Buckinghamshire UB8 1DH, England

Salary

£60,000 - £72,000 per annum

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Contract type

Full Time

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.

Sonic Summary

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  • Gibbs Hybrid is seeking a Global Clinical Supply Chain Manager for a remote role based in Uxbridge, responsible for managing the supply portfolio of clinical studies.
  • The role requires creating and maintaining supply strategies for investigational products while demonstrating strong knowledge of clinical supply chain processes.
  • Candidates must have pharma industry experience, with a focus on global clinical supplies and development, along with strong analytical and project management skills.
  • The position involves developing supply forecasts, monitoring inventory, and acting as the main contact for clinical supplies related to assigned studies.
  • The expected salary for this role is competitive, and candidates should have a minimum of 5 years of relevant experience.

Global Clinical Supply Chain Manager - Remote/Uxbridge

Gibbs Hybrid is looking for an accomplished Clinical Supply Chain Manager to manage the global supply portfolio of clinical studies. You will create and maintain supply strategies for all investigational products based on the scientific and regulatory confines of the drug’s development with minimal supervision.

• Proactively defines, plans, and communicates the clinical supply chain strategy in support of global clinical studies to promote optimal use and alignment with study and corporate goals. Demonstrates strong knowledge of GCSC processes when presenting at cross-functional meetings.

• Responsible for identifying and supporting strategies for continuous improvement, both departmental and/or inter-departmental.

• Influences clinical and development timelines, study design and country selection. Directly responsible for reviewing and providing input to draft clinical protocols

• Develops supply forecasts for studies through evaluation of the clinical development plan and protocol analysis. Monitors inventory and analyses drug utilization versus forecast taking into account country requirements and logistical timelines.

• Issues Manufacturing and Packaging/Labelling requests to Clinical Supply Operations

• Monitor use date of investigational drug product for assigned protocols.

• Actively participates in internal Trial Supply Management and Clinical Supply Chain meetings

• Acts as the main Clinical Supplies contact person for the assigned compound and associated studies, leading communications regarding global supply strategy with study team as appropriate.

Essential:

• Pharma industry related experience.

• Global Clinical Supplies/Development experience.

• Knowledge of the global drug development process and global regulatory requirements.

• Proficient and strong analytical skills.

• Project management and global supply chain skills, within pharma ideally, or equivalent

• Strong knowledge of Forecasting and Planning and proficient knowledge of related areas, i.e. Manufacturing, Packaging & Labelling, IVRS, Logistics, Quality, Stability, etc.

• Proficient knowledge of import / export requirements.

• Knowledge/experience of IVRS and CTMS systems, a benefit

• Translates broad strategies into specific objectives and action plans.

• Team and individual leadership (leads courageously).

• Negotiation (Manages Execution, Results Driven, Analysis of Issues, Effective Speaking, Builds Relationships).

• Influencing (manages influencing others).

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In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.