This role ensures consistent product availability while optimising inventory across Europe, the Middle East, and Africa.
The Advocate Group are proud to be partnering with a global FMCG business, looking for a qualified Supply Chain professional to join their busy EMEA team.
As a Supply Planner that will be part of the EMEA Operations Planning Team located in London, you will be responsible for meticulously planning, processing, and managing finished goods purchase orders to maintain optimal stock levels.
Contract Duration: 12 Months Flex to be extended/perm
Global Clinical Supply Chain (CSC) is a new organization within Global Supply Chain (GSC).
GSC's vision is to be a patient-centric, integrated supply chain, launching and supplying innovative products that deliver hope to patients through life-changing medicines.
Gibbs Hybrid is looking for an accomplished Clinical Supply Chain Manager to manage the global supply portfolio of clinical studies.
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.
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.
Responsibilities: Lead and manage the reporting and performance of the management P&L against agreed targets and the business planning processes to ensure robust business plans are submitted for Specialty Business Division (SBD) and Corporate Divisions (Corporate Functions and Global Functions).
Company: Our client is a leading international pharmaceutical business based in Uxbridge, Middlesex
Posted by Parkside Office Professional • £350/day to £360/day
Experience in Primary Analysis and data analysis in general - Familiar with PFS and OS analysis, imaging management in oncology Clinical trials, ePRO management.
Clinical Trials Manager - Oncology 12 month contract Location Stockley Park (3 days onsite required) An experienced CTM with extensive oncology (preferably solid tumours) experience.
Clinical Operations is responsible for the worldwide execution of all Phase I - IV clinical trials across all therapeutic areas.