Pharmaceutical Regulatory Affairs Jobs in Maidenhead

Consult - Maidenhead, United Kingdom

• Oversee a portfolio of CTAs, managing the preparation and dissemination of documentation for new initial CTAs and all CTA maintenance activities, including substantial amendments and end-of-trial notifications...

from: uk.lifeworq.com - 3 days ago

Consult - Maidenhead, United Kingdom

Develop and execute CTA regulatory strategies and operations for a designated portfolio of developmental compounds across specified regions: WE, EEMEA, LA, and select JAPAC countries, ensuring alignment...

from: uk.lifeworq.com - 22 days ago

Park Street People - Uxbridge, London, United Kingdom

Strong communication and stakeholder management experience, you will be able to demonstrate working in project teams, where you have guided/advised on the implementation of your strategy/regulatory plan... £46 - £48/hour

from: CV-library.co.uk - 5 days ago

Consult - Maidenhead, United Kingdom

• Oversee a portfolio of CTAs, managing the preparation and dissemination of documentation for new initial CTAs and all CTA maintenance activities, including substantial amendments and end-of-trial notifications...

from: uk.lifeworq.com - 22 days ago

Cpl Life Sciences - Slough, United Kingdom

As a Regulatory Affairs Professional, you will assume a crucial role in providing leadership and expertise in all regulatory and submission-related aspects of clinical trials. You will serve as the main...

from: uk.lifeworq.com - 22 days ago

Parexel - Uxbridge, United Kingdom

When you join us, you’re joining a team that sees everything they do as an opportunity to transform the world for patients everywhere. When our employees bring their many perspectives together to tackle... Competitive

from: pharmiweb.jobs - 3 days ago

Veterinary Medicines Directorate - Addlestone, United Kingdom

This exciting and interesting job puts you at heart of authorising veterinary medicines for the UK market and plays a major role in assuring the quality and hence the safety and efficacy of these medicines...

from: uk.lifeworq.com (+2 sources) - 5 days ago

Cpl Life Sciences - Uxbridge, United Kingdom

Manages strategy and execution for all regulatory CMC submissions (e.g. late-stage clinical trials, variations, extensions and marketing applications) for products within the portfolio in compliance with...

from: uk.lifeworq.com - 3 days ago

Uxbridge, England, United Kingdom

As the CMC Regulatory Manager, you will play a vital role in our company's worldwide post-approval regulatory activities, specifically focused on Chemistry, Manufacturing, and Controls (CMC) for biological...

from: jobleads.co.uk - 18 days ago

slough, england, United Kingdom

Work in collaboration with Clinical Development Quality, Patient Safety, Regulatory Affairs, strategic partners, and other stakeholders to ensure compliance with International Council for Harmonization...

from: jobleads.co.uk - More than 30 days ago