Our client is a global biotechnology company specialising in the development of immunological products to diagnose and monitor patients with immunologically controlled diseases.
The role
An opportunity has become available for an Regulatory Specialist, experienced in Diagnostics, to join company and support the Global Regulatory activities in order to facilitate timely approval of new and existing products.
The Group Compliance Function's aim is to proactively support Willis Towers Watson to generate sustainable value, helping the company to deliver good client outcomes, manage its conduct, protect against regulatory risk, and to maintain strong regulatory relationships.
We aim to be a trusted partner to the business.
Within Willis Towers Watson's internal control system, we form part of the Second Line of Defence, as a function independent from daily business activities.
SRG are currently looking for Regulatory Specialist for a Global Pharmaceutical Company who have opened new vacancies within their Regulatory team on an initial 12 Month basis to be based at their office in Maidenhead/Remote.
The Role
The Regulatory Associate is responsible for providing global regulatory expertise for Clinical Trials.
They are the primary interface between global functions and affiliates to deliver clinical development regulatory strategies, operations and outcomes.
We are currently recruiting for two Regulatory Specialists to join a Milton Keynes based company, in a 1-year fixed term contract.
Overview
You will need to:.
The successful candidate will support internal customers including: Customer Service team, Sales reps, Research & Development team, and Quality Assurance team by serving as an expert in assigned areas.
An accountancy and business advisory firm, providing the advice and solutions entrepreneurial organisations need to navigate today's changing world.
We work with the companies that are Britain's economic engine - ambitious, entrepreneurially-spirited and high-growth businesses that fuel the economy - and directly advise the owners and management teams that lead them.
This biotech is looking to strengthen their Regulatory Labelling group by taking on an experienced Regulatory Labelling professional for a contract job based in West London.
Regulatory Affairs Labelling Manager; Your new company
This consultancy is looking to strengthen their Regulatory Labelling group by taking on an experienced Regulatory Affairs Labelling professional for a contract job.
This job is outside IR35 and has scope for extension.
This is an excellent opportunity for an experienced Clincial Trial Regulatory Specialist to join a global pharmaceutical company for an initial 12 months with the potential for this to be extended.
This role has come about due to expansion and an increase in the production of pharmaceutical.