Regulatory Affairs Consultant jobs in London

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REGULATORY AFFAIRS MANAGER - PRECISION MEDICINE (UK OR AUSTRIA)

Our Development Team is guided by our purpose: to reimagine medicineto improve and extend peoples lives. We are investing in new technologies and building specific therapeutic area and platform depth and capabilities all to br...

CompanyNovartis
AddressLondon, England
CategoryScientific
Job typeRegular
Date Posted 2 days ago See detail

Regulatory Affairs Manager - Precision Medicine (UK or Austria)

Novartis

London, England

Our Development Team is guided by our purpose: to reimagine medicineto improve and extend peoples lives. We are investing in new technologies and building specific therapeutic area and platform depth and capabilities all to br...

Regulatory Affairs Systems & Strategy Manager

Novartis

London, England

Our Regulatory Operations Team is guided by our purpose: to reimagine medicineto improve and extend peoples lives. We are investing in new technologies and building specific therapeutic area and platform depth and capabilities...

Global Regulatory Affairs Manager Medical Devices (UK or Austria)

Novartis

London, England

Our Development Team is guided by our purpose: to reimagine medicineto improve and extend peoples lives. We are investing in new technologies and building specific therapeutic area and platform depth and capabilities all to br...

Senior Regulatory Affairs Coordinator

Novartis

London, England

Our Development Team is guided by our purpose: to reimagine medicineto improve and extend peoples lives. We are investing in new technologies and building specific therapeutic area and platform depth and capabilities all to br...

Senior Manager Regulatory Affairs Process Excellence

Novartis

London, England

Our Development Team is guided by our purpose: to reimagine medicine to improve and extend peoples lives.To do this, we are optimizing and strengthening our processes and ways of working. We are investing in new technologies and...

Regulatory Affairs Manager

Proclinical Staffing

London, Greater London

GBP400 - GBP500 per hour

Assist in the preparation of new local regulatory guidance documents. Manage initial Marketing Authorisation applications, Variations and other MA maintenance applications. Ensure timely and compliant filing of clinical trial appl...

CMC Regulatory Affairs Manager

Park Street People

Uxbridge, Greater London

£40 - £43/hour

A key role in the execution of CMC regulatory strategies working on multiple cross functional projects. Oversee all regulatory submissions as well as reviewing and altering dossiers as necessary ensuring that these are compliant....

Regulatory Affairs Senior Manager

Proclinical Staffing

Uxbridge, Greater London

GBP60 - GBP70 per hour

Advise the Global Regulatory Team on considerations in strategy development for each region. Manage submissions for products in compliance with local regulations. Lead the expansion of regional regulatory documents and meetings in...

Regulatory Affairs Manager

Proclinical Staffing

London, Greater London

GBP48 - GBP55 per hour

This role involves supporting multiple products from a global and international regulatory perspective. Responsibilities:- Generate country-specific regulatory strategies and provide feedback to internal teams regarding submission...

Sr Manager Regulatory Affairs

I-Pharm Consulting

London, Greater London

GBP58 - GBP64 per hour + -

Strategic Guidance: Advise the GRT on regional considerations to ensure regional needs are defined and implemented in collaboration with relevant stakeholders. Management: Potentially supervise one or more regional regulatory lead...

Regulatory Affairs Manager

I-Pharm Consulting

London, Greater London

GBP40 - GBP55 per hour + NA

Advise the GRT on regional strategy development. Implement regional needs with stakeholders. Supervise regional regulatory leads or support staff. Liaise with regulatory agencies and communicate outcomes. Manage regulatory submiss...

Regulatory Affairs Specialist

Astrazeneca

London, England

UK Regulatory experience Ability to work independently on regulatory submissions and approvals throughout the product lifecycle in a timely manner Drive meaningful interactions with cross-functional teams within the UKMC as well a...