REGULATORY MANAGER CLINICAL TRIALS jobs in UNITED KINGDOM, United Kingdom #2

role in providing leadership and expertise in all regulatory and submission-related aspects of clinical trials..., amendments, and strategies Provide leadership and expertise in regulatory and submissions-related aspects of clinical trials...

CK Group are recruiting for a Senior Manager Regulatory Affairs to join a biopharmaceutical company who are based in... to support clinical trials for investigational medicinal products as well as to market approved medicinal products to ensure...

CK Group are recruiting for a Senior Manager Regulatory Affairs to join a biopharmaceutical company who are based in... to support clinical trials for investigational medicinal products as well as to market approved medicinal products to ensure...

for regulatory submissions regarding: Clinical trial applications; New marketing applications; HA responses & background packages... (including participating / leading HA meetings); &/or post-approval submissions. In this role, the CMC Regulatory Manager...

accurate preparation of high-quality regulatory documents needed to support clinical trials and medical products. Contributing...A global pharmaceutical company, based in Uxbridge is currently looking for a Senior Regulatory Affairs Manager...

of London, England Posting date: 10 May 2024 Reference: 60310 UK CW Regulatory Affairs Manager (Inside IR35) This role... for submission in the relevant countries Manages strategy and execution for all regulatory CMC submissions (e.g. late stage clinical...

CK Group are recruiting for a Regulatory Affairs Manager CMC to join a biopharmaceutical company who are based in... for submission in the relevant countries. Manage strategy and execution for all regulatory CMC submissions (e.g. late stage clinical...

CK Group are recruiting for a Regulatory Affairs Manager CMC to join a biopharmaceutical company who are based in... for submission in the relevant countries. Manage strategy and execution for all regulatory CMC submissions (e.g. late stage clinical...

and expertise in all regulatory and submission-related aspects of clinical trials. You will serve as the main point..., and strategies Provide leadership and expertise in regulatory and submissions-related aspects of clinical trials...

CK Group are recruiting for a Regulatory Affairs Manager to join a biopharmaceutical company who are based in Uxbridge... are acquired and maintained in order to support clinical trials for investigational medicinal products as well as to market...

++ Regulatory Affairs Manager – 12 month contract (inside IR35) ++ Within this role you will support... of the role: Ensure that the client acquires and maintains all the required approvals in order to support clinical trials...

CK Group are recruiting for a Regulatory Affairs Manager to join a biopharmaceutical company who are based in Uxbridge... are acquired and maintained in order to support clinical trials for investigational medicinal products as well as to market...

Job Purpose The Senior Manager, Medical & Regulatory Writing will be an integral part of MoonLake’s Clinical.... Key Accountabilities: Lead scientific contribution to the development of medical, regulatory and clinical documents...

Job Purpose As a Senior Manager, Regulatory Affairs CMC, you are an integral part of MoonLake’s Clinical Development... Senior Manager, Regulatory Affairs CMC will serve as a subject matter expert, which will involve collaborating with multiple...

for a Senior Manager - Regulatory Affairs to work within the Global Regulatory Affairs - Innovative Medicines (Europe) team.... We have a hybrid approach to home working! A day in the life of a Senior Manager Regulatory Affairs... You will develop regulatory...

relating to medicinal products. Understanding of the regional regulatory procedures for clinical trials, marketing...Proclinical is seeking a dedicated Regional Regulatory Lead to support one or more products from a regional regulatory...

procedures for clinical trials, marketing authorizations, post-approval changes, extensions, and renewals. Strong knowledge... Uxbridge, England Posting date: 24 May 2024 Reference: 60570 Proclinical is seeking a dedicated Regional Regulatory Lead...