Clinical Trial Supplies Manager
£28.76 ph. This role is inside IR35. Clinical Trial Supplies Manager Role: Collaborate with internal Global Clinical Supply Chain (GCSC) teams and external Customers and Service Providers.
Proactively defines, plans, and communicates the clinical supply chain strategy in support of global clinical studies.
Responsible for identifying and supporting strategies for continuous improvement.
Ensures timely delivery of quality clinical supplies for all assigned compounds and protocols.
Participates in the development, review and approval of Interactive Response Technology (IRT) specifications. Develops investigation product distribution strategies and maintains distribution and supply strategies at depot and site level according to study.Your Background: Previous working experience in Clinical Supplies.
Knowledge of global drug development process and global regulatory requirements.
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.
Ability to translate broad strategies into specific objectives and action plans. Company:
Our client is the global leader in enabling pharma, biotech, and consumer health partners to optimise product development, launch, and full life-cycle supply for patients around the world. They have the goal of putting patients first and to help people around the world live better and healthier lives. Location:
This role is home-based, with one or two trips to Uxbridge per month. Apply:
For more information, or to apply for this Clinical Trial Supplies Manager please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference (Apply online only). It is essential that applicants hold entitlement to work in the UK Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check. INDKA
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