Manage the business planning processes to ensure robust business plans are developed for Corporate Divisions (Corporate Functions and Global Functions).
Lead and oversee the reporting and performance of the management P&L against agreed targets.
Global Clinical Supply Chain (CSC) is a new organization within Global Supply Chain (GSC).
Contract Duration: 12 Months Flex to be extended/perm
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.
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
This role is expected to be worked on a hybrid basis but remote applications will also be considered.
Our client, a global pharmaceutical company, is currently looking for a Clinical Trials Supply Chain Manager to join their team in Uxbridge on a full time, 12-month temporary basis (35 hours per week).
You will be responsible for managing the supplies for the clinical trials and/or drug development whilst ensuring that this is done in a cost-effective and timely manner.
Working with the regulatory team (and core stakeholders across multiple areas), your role will be to provide regulatory strategy and guidance across the region and make sure that regulatory deadlines and approvals are achieved.
An innovative global pharmaceutical company is currently looking for a Regulatory Affairs Manager with CTA, EU and early stage development experience to join their team on a 12 month temporary contract.
Other responsibilities include
You will develop, contribute and ensure the accurate preparation of high-quality regulatory documents needed to support clinical trials and medical products.
Our client, a global pharmaceutical company is currently looking for a Senior Regulatory Affairs Portfolio Manager to join their team based on the outskirts of London on a full time, 8-month temporary basis (35 hours per week).
This opportunity will see you working with senior stakeholders to develop, execute and deliver the regulatory strategy for assigned products.
This is a remote-by-design role which will require flexibility to attend key meetings on-site (Uxbridge).