REGULATORY MANAGER CLINICAL TRIAL jobs in United Kingdom #2

and collaborative environment. The Global Trial Manager (GTM) role sits in the Clinical Program Operations (CPO) function, alongside... and innovative clinical trial portfolio on time and on budget and in accordance with quality standards. No day will be the same...

Amgen

of Global Trial Optimisation. This role involves overseeing the clinical development strategy, clinical study concepts... clinical trial operations, including experience developing protocols and key study documents. - Technical proficiency in...

Proclinical

Reference Number: JO-2405-535693 Regulatory Affairs Manager Rate: £50,000 – 65,000 Job Type: Permanent Location...: Central London / West End Job Title: Regulatory Affairs Manager (CTA/ CTR) Job Type: Permanent, full-time Locations: UK...

Clinical Professionals

in a scientific discipline Background in clinical trial management Experience in Regulatory Affairs Good...Reference Number: JO-2404-532643 Regulatory Strategy and Submissions Manager Rate: Negotiable Job Type: Contract...

Clinical Professionals

(MA) applications, variations, and other MA maintenance applications. Timely and compliant filing of clinical trial applications..., amendments, and other clinical trial submissions. Reviewer for promotional and non-promotional activities and materials...

Actalent

(MA) applications, variations, and other MA maintenance applications. Timely and compliant filing of clinical trial applications..., amendments, and other clinical trial submissions. Reviewer for promotional and non-promotional activities and materials...

Actalent

, and other MA maintenance applications. Timely and compliant filing of clinical trial applications, amendments, and other clinical trial... on a range of regulatory topics Able to work equally well as part of a team or independently Job Title: Regulatory Affairs Manager...

Actalent

. The successful candidate will support the local execution of the EU regional regulatory strategy, including clinical trial...Proclinical is seeking a dedicated and experienced Manager for Regulatory Affairs. This role will focus on the local...

Proclinical

regional regulatory strategy, including clinical trial application submissions and the affiliate commercial strategy.... Ensure timely and compliant filing of clinical trial applications, amendments, and other clinical trials submissions. Review...

Proclinical

(MA) applications, variations, and other MA maintenance applications. Timely and compliant filing of clinical trial applications..., amendments, and other clinical trial submissions. Reviewer for promotional and non-promotional activities and materials...

Actalent

. For new clinical trial and regulatory project proposals and ongoing projects, provide regulatory intelligence in support... that could impact the strategy and execution of regulatory, integrated product development, and clinical trial projects. Assess the...

Rho

We have an opportunity for a Senior Regulatory Manager within the Clinical Development team. You will be a highly skilled and experienced... regulatory expert, with recent hands-on experience of successful clinical trial submissions within the Latin America and/or Asia...

Bionical Emas

local and EU regulatory strategy, including the management of marketing authorisations, clinical trial application... Cambridge, England Posting date: 06 Jun 2024 Reference: 60789 Proclinical is seeking a Regulatory Affairs Manager...

Proclinical

to medicinal products. Understanding of the regional regulatory procedures for Clinical Trial Applications, Marketing... professional for the role of Regulatory Affairs Senior Manager. The successful candidate will be responsible for providing...

Proclinical

CK Group are recruiting for a Senior Manager Regulatory Affairs to join a biopharmaceutical company who are based in...., clinical trial and marketing applications) for assigned products in accordance with global filing plans, core labelling...

CK Group

CK Group are recruiting for a Senior Manager Regulatory Affairs to join a biopharmaceutical company who are based in...., clinical trial and marketing applications) for assigned products in accordance with global filing plans, core labelling...

CK Group

. Job Description Senior Manager, Regulatory Affairs – UK and Ireland Holborn Gilead Sciences, Inc. is a research-based biopharmaceutical... initial MAA’s, post-MA activities and clinical trial application (CTA) submissions, in alignment with the UK and Ireland...

Gilead