REGULATORY MANAGER jobs in UXBRIDGE GREATER LONDON, United Kingdom

Position: Regulatory Affairs Manager Location: Uxbridge (UK) Contract Length: 6-month (View to extend) Work... Structure: Monday - Friday Pay Rate: Available on request - (Inside IR35) The new Regulatory Affairs Manager...

Proclinical is seeking a dedicated Regulatory Affairs Manager. This role involves supporting multiple products... from a global and international regulatory perspective. The successful candidate will be responsible for generating country-specific...

Regulatory Affairs Manager CMC Duration: 6 month Contract Inside IR35 Location: Uxbridge, 3 days on-site per week..., and Controls (CMC) within regulatory affairs. Responsibilities include: Leading global regulatory strategies...

Position: Sr Manager Regulatory Affairs Work Structure: Monday - Friday, 39 hours per week Pay Rate: £58 - £64/hour... (Inside IR35) Job Description: We are seeking a seasoned Sr. Manager of Regulatory Affairs to support one or more products...

CK Group are recruiting for a Senior Manager Regulatory Affairs to join a biopharmaceutical company who are based in... timely regulatory compliance with above approvals. Advise the Global team on regional considerations in developing strategy...

CK Group are recruiting for a Senior Manager Regulatory Affairs to join a biopharmaceutical company who are based in... timely regulatory compliance with above approvals. Advise the Global team on regional considerations in developing strategy...

(including participating / leading HA meetings); &/or post-approval submissions. In this role, the CMC Regulatory Manager... lives. Read more: Functional Area Description The GRS-CMC organization provides regulatory expertise related to CMC...

A global pharmaceutical company, based in Uxbridge is currently looking for a Senior Regulatory Affairs Manager... to join their team. You will be a confident Regulatory Lead looking to work in an innovative therapy area, developing and defining...

Regulatory Affairs Manager (Inside IR35) Duration: 12 months (Extention possible) Location: Uxbridge, 3 days... Affairs Manager, where you'll support regional regulatory activities for innovative products. As a key member of the Global...

lives. Read more: Position summary The Manager I will be responsible for supporting the RISM business lead for GRS... is a plus Proficient knowledge of global regulatory practices, submission guidelines and requirements. Identifies and resolves issues...

CK Group are recruiting for a Regulatory Affairs Manager CMC to join a biopharmaceutical company who are based in... Rate: £45.02phr PAYE. Role: Responsible for the generation of country specific regulatory strategies and providing...

Our client, a global pharmaceutical company, is currently looking for a CMC Regulatory Affairs Manager.... Key Responsibilities A key role in the execution of CMC regulatory strategies working on multiple cross functional...

CK Group are recruiting for a Regulatory Affairs Manager CMC to join a biopharmaceutical company who are based in... Rate: £45.02phr PAYE. Role: Responsible for the generation of country specific regulatory strategies and providing...

CK Group are recruiting for a Regulatory Affairs Manager to join a biopharmaceutical company who are based in Uxbridge... will support one or more products from a regional regulatory perspective and will achieve the desired labelling by developing...

CK Group are recruiting for a Regulatory Affairs Manager to join a biopharmaceutical company who are based in Uxbridge... will support one or more products from a regional regulatory perspective and will achieve the desired labelling by developing...

An innovative global pharmaceutical company is currently looking for a Regulatory Affairs Manager with CTA, EU... and early stage development experience to join their team on a 12 month temporary contract. Working with the regulatory team...

Trial Manager LIVE What you will do In this vital role you will be responsible for successfully delivering... accordance with Regulatory Authorities, company SOPs and ICH-GCP guidelines including Trial Master File (TMF) Management...