Posted by Oxby and Parke Recruitment • £40K/yr to £45K/yr
General
Hybrid working pattern: 1 day in the office and 4 remote.
The Company
A rapidly expanding, European Financial Services business.
Dues to continued growth, the Business Transformation Team require additional support, likely until the end of 2024 but with potential to extend beyond.
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.
Posted by Jackie Wilsher Staff Service • £30K/yr to £50K/yr
We are currently recruiting for a Senior Buyer on a temporary basis.
Working with Engineering and Operations teams to arrange timely supply of approved materials at cost effective prices whilst maintaining quality and delivery requirements.
This is a rolling contract so we cannot confirm the length of the temporary booking.
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.
This role is expected to be worked on a hybrid basis but remote applications will also be considered.
Posted by Hays Specialist Recruitment Limited • £450/day to £550/day
Your new company
With this project in particular, you will be providing commercial support on an £80 million project which involves work on a dual-carriage road and roundabouts.
You will be working for an award-winning and widely recognised Tier One contractor who delivers high quality work on road schemes, partnering with National Highways and local authorities.
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.
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.
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.