Drug Regulatory Affairs Jobs in Hatfield

CK Group- Science, Clinical and Technical - Uxbridge, United Kingdom

Provide regulatory direction on regional regulatory mechanisms to optimise product development (e.g. expediting FIH studies, Orphan Drug, conditional/accelerated approvals, compassionate use and paediatric... £0 - £48.92/hour

from: CV-library.co.uk (+2 sources) - 9 days ago

SEC Life Sciences - Hitchin, United Kingdom

Lead and manage projects involving Real World Evidence (RWE), integrating these insights with Regulatory Affairs to optimise early access programmes. Design and implement strategies to gather and utilise...

from: uk.lifeworq.com (+2 sources) - 9 days ago

London, England, United Kingdom

· Be responsible for executing and effective quality control reviews and tracking (primarily) internally used labeling documents (Core Data Sheet, Core Patient Information Leaflet, Core Instructions for...

from: jobleads.co.uk - 5 days ago

London, England, United Kingdom

Define and lead the regulatory CMC dossiers strategy, content and appropriateness for the respective development and commercial products (lifecycle maintenance); coordinate the preparation and review the...

from: jobleads.co.uk - 5 days ago

ClinChoice - London, United Kingdom

Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately... Competitive

from: pharmiweb.jobs (+1 source) - 8 days ago

London, England, United Kingdom

Provide input, as required, into regulatory strategy and timeline development for new study opportunities Assists in establishing company standards to ensure the highest quality of submitted information...

from: jobleads.co.uk - 7 days ago

London, England, United Kingdom

Identify and guide the preparation and submission of documentation to relevant region regulatory bodies such as Therapeutic Goods Administration (TGA) in Australia, Food and Drug Administration (FDA) in...

from: jobleads.co.uk - 11 days ago

AbbVie - Maidenhead, United Kingdom

In collaboration with applicable GXP RDQA Leaders, lead, develop and implement routine and QA oversight strategies relating to R&D business stakeholders including but not limited to Pharmacovigilance and...

from: europharmajobs.com - 10 days ago

High Wycombe, England, United Kingdom

The Senior Manager Regulatory Affairs (RA) leads a team responsible for the development of CMC/technical regulatory strategies across the EMEA region providing regulatory input and technical guidance on...

from: jobleads.co.uk - 6 days ago

GlaxoSmithKline - Brentford, UK

Accountable to Senior Director of Respiratory Established Products and VP, Global Regulatory Established Products for development of appropriate global and/or regional regulatory life cycle strategy(s)...

from: vercida.com - Yesterday