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Keywords: Global Regulatory Lead Pharmaceutical Development, Location: London

Page: 5

Senior Principal Statistical Programmer

position is a key collaborator and strategic partner with biostatistics in ensuring that pharmaceutical drug-development plans... in Novartis Global Drug Development are executed efficiently with timely and high-quality deliverables. This role offers hybrid...

Company: Novartis
Location: London
Posted Date: 06 Dec 2024

Principal Statistical Programmer

with biostatistics in ensuring that pharmaceutical drug-development plans are executed efficiently with timely and high-quality... deliverables in Novartis Global Drug Development. This role offers hybrid working, requiring 3 days per week in our Basel office...

Company: Novartis
Location: London
Posted Date: 06 Dec 2024

CMC Technical Documentation Specialist, Technical Operations

Specialist will be a member of the Global Technical Development team and will be responsible for preparing and drafting CMC... source documents for use in global regulatory filings such as Investigational New Drug (IND) Applications, Investigative...

Location: London
Posted Date: 02 Dec 2024

MS&T Analytical Manager

method development, validation, transfer, statistical analysis, and data visualisation aligning with global regulatory... biopharmaceutical group specialising in the development of innovative medicines in oncology, neuroscience, and rare diseases. Our goal...

Company: Ipsen
Location: London
Posted Date: 07 Nov 2024

Client Advice Manager, 6 Month FTC

. We are liberated by a global structure which is designed to deliver highly differentiated and highly effective communications...'s lives. OUR MISSION AND VALUES Our reason to exist is ambitiously simple: To enhance the health of global citizens...

Company: Mediabrands
Location: London
Posted Date: 06 Nov 2024

Senior Medical Writer (Remote)

submissions that meet rigorous regulatory standards. With a global footprint across four continents, MMS maintains a 97 percent... years of previous experience in the pharmaceutical industry Must have at least 3-5 years of industry regulatory writing...

Company: MMS
Location: London
Posted Date: 03 Nov 2024

Principal Medical Writer - Remote

partner, creating compelling submissions that meet rigorous regulatory standards. With a global footprint across four... protocol experience, as lead author, required Experience leading and managing teams while authoring regulatory documents...

Company: MMS
Location: London
Posted Date: 30 Oct 2024