Drug Regulatory Affairs Jobs

ClinChoice - London, United Kingdom (+1 location)

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 (+2 sources) - 9 days ago

United Kingdom

Minimum five years of experience in Regulatory Affairs related to medical devices, drugs and/or biologics, developing regulatory deliverables and submissions. Work experience must include writing and/or...

from: jobleads.co.uk - 6 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 - 6 days ago

ICON Plc - United Kingdom, Homeworking

Contribute to at least two of the following areas: Interactions with Regulatory agencies, early phase consulting, Development Planning (PDP/RDP/CDP), Scientific/Agency advise, orphan drugs/pediatric development... Competitive

from: pharmiweb.jobs - 11 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 - 7 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 - 8 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 - 11 days ago

Scendea

Support Scendea's Business Development in sales/marketing introductions, preparation of project proposals & educational materials, review written estimates, quotations and contracts for Clients as required...

from: joblookup.com (+1 source) - 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 - 12 days ago

Parexel - United Kingdom

Solid aptitude for use of IT systems; Regulatory Information Management System (RIMS), electronic document management system (EDMS). Ability to manage the review and approval of labeling in a document... Competitive

from: pharmiweb.jobs (+1 source) - 23 days ago