Manager, Trial Supplies managementCK Group are recruiting for a Manager - Trials Supplies Management to join a global pharmaceutical company, based in Uxbridge on a contract basis for 12 months.
Salary: Paying an Hourly rate up to £28.76 per hour PAYE Manager, Trial Supplies Management Role: Collaborate with internal Global Clinical Supply Chain teams and external Customers and Service Providers, including but not limited to Global Drug Development, Pharmaceutical Development, Product Development Quality (PDQ), External Vendors and Medical to ensure all needs are met.Proactively define, plan, and communicate the clinical supply chain strategy in support of global clinical studies to promote optimal use and alignment with study and corporate goals.Responsible for identifying and supporting strategies for continuous improvement, both departmental and/or inter-departmental.Influence clinical and development timelines, study design and country selection.Directly responsible for reviewing and providing input to draft clinical protocols, communicating timelines and investigational product strategies to study and cross-functional teams.Develop supply forecasts for studies through evaluation of the clinical development plan and protocol analysis.
Monitor inventory and analyze drug utilization versus forecast taking into account country requirements and logistical timelines.Issue Manufacturing and Packaging/Labeling requests to Clinical Supply Operations (CSO) in alignment with RDSC Master Planning timelines and based on collaboration with Clinical Development team, Chemistry, Manufacturing & Controls (CMC) team and CSO Packaging and Labeling to ensure package design and clinical label for investigational product meet protocol and regulatory requirements.Monitor use date of investigational drug product for assigned protocols.
Your Background: Minimum 2 years Pharma industry related experience.Minimum 1 years Clinical Supplies/Development with global experience or equivalent experience.Moderate / Strong knowledge of the global drug development process and global regulatory requirements.Strong knowledge of Forecasting and Planning and proficient knowledge of related areas, i.e.
Manufacturing, Packaging & Labeling, IVRS, Logistics, Quality, Stability, etc.Proficient knowledge of import / export requirements.Proficient/Strong knowledge of IVRS and CTMS systems.Proficient / Strong knowledge of industry technology.
Company: Our client is the global leader in enabling pharma, biotech, and consumer health partners to optimize 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 remote based in the UK and the clients site is in Uxbridge.