UK CW Regulatory Affairs Manager - remote

Highly Competitive
  1. Contract
  2. Project Manager
  3. United Kingdom
City of London, England
Posting date: 10 May 2024

UK CW Regulatory Affairs Manager (Inside IR35)

This role will support one or more products from a regional regulatory perspective.
* Responsible for the generation of country specific regulatory strategies and providing feedback to internal teams regarding submission plans and execution of the strategy for one or more products.
* Interfaces with affiliate offices for specific strategies or activities that impact a specific country.
* Ensuring CMC regional issues impacting global regulatory strategy for proposed CMC filings are considered and risks identified with appropriate contingency strategies
* Review the preparation of M2 and 3 CMC components of filings and assess fitness of purpose for submission in the relevant countries
* Manages strategy and execution for all regulatory CMC submissions (e.g. late stage clinical trials, variations, extensions and marketing applications) for products within company's portfolio in compliance with global filing plans and local regulatory requirements with minimal supervision.
* Authoring and coordinating responses to questions across assigned products and countries.
* Communicate regional needs for ensuring reliability of the supply chain and successful launch are well defined and implemented in collaboration with relevant regional stakeholders
* Provides guidance for regulatory assessments of change control requests
* Sets project timeframes and priorities for products under their responsibility based on project objectives and ongoing assignments; raises resource constraints
* Gathering, consolidating and analyzing regulatory intelligence for International Markets and supports its application to product-specific activities
* Share regulatory information and implications with the stakeholders on an ongoing basis and provide advice on regional considerations
* Maintain an awareness of new and developing legislation, regulatory policy and technical Regulatory guidance relating to company products.
* Performs regulatory research to obtain relevant histories, precedence and other information relevant to regional product advancement.

If you are having difficulty in applying or if you have any questions, please contact Caitlin Siljeaur at

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.