Associate Director Supply Chain
- Permanent
- Technical Operations, Supply chain, Logistics
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Hobson Prior are looking for an Associate Director Supply Chain to join a biopharmaceutical research organisation who specialize in oncology product development and pioneering medicines that are used all over the world. This role will manage the clinical supply activities for assigned clinical programs.
Job Responsibilities:
- Develop and maintain clinical supply and inventory plans for assigned programs; leads cross-functional clinical supply status meetings.
- You will represent Clinical Supply Chain on Clinical Study Teams and provide a high service level to internal stakeholders.
- Coordinate sourcing of co-meds working closely with Procurement and Clinical Operations.
- Co-operate with Clinical Operations to understand clinical demand requirements and ensures alignment with study teams on clinical supply plans and timelines.
- Accountable to generate and monitor co-med budgets and spend working closely with Clinical Operations and Finance.
- You will ensure delivery of co-meds to Clinical Operations and Technical Operations for further packaging and distribution.
- Manage the relationship and oversee daily activities for co-med sourcing vendors.
- Manages clinical supply inventory, develops inventory reports and monitors upcoming expiry for assigned programs.
- Coordinate efforts between Project Management, Clinical Operations, Technical Operations and maintains forecast and timelines for clinical supplies for assigned programs.
- Maintain routine and timely communication with Technical Operations of any changes in clinical supply forecasts or study timelines.
- Facilitate discussions and decisions on label and packaging design, as needed.
- Support IRT user acceptance testing, develops IRT supply strategy, and oversees ongoing supply activities in the system.
Key Skills:
- Strong organizational, analytical, problem solving, and communication skills.
- Must be a dependable self-starter and be capable of working independently on multiple projects with the ability to prioritize tasks and meet deadlines.
Requirements:
- Bachelor degree in a related field.
- A minimum of 3-4 years of work experience in the pharmaceutical industry.
- Prior experience in clinical supply chain and/ or clinical study operations is required.
- Knowledge of global clinical trials and the drug development process.
- Knowledge of global pharmaceutical regulatory requirements (e.g. cGMP, GCP).
- Knowledge of IRT system set up and functionality and proficiency with Excel modeling.
- Competence with computers and technology is essential; to include extensive experience with MS Office Applications is required.
- Experience with forecasting and inventory management tools is preferred
- Experience in vendor oversight and managing external partnerships.
Apply now:
If you are interested in learning more or applying to this exciting opportunity, please complete the form below and attach a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist, please request a call back at the top of this page.
Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.
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