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Full-time permanent opportunity to join our client as a Medical Manager & Final Signatory - competitive package available
An exciting opportunity to join a vibrant & growing Co, ensuring compliance with MHRA guidelines & GDP, excellent knowledge of UK and EU legislation.
Minimum 12 month contract for a medical affairs / MSL professional to work in Cardiology - remote working with some UK travel and meetings in Surrey
We have a fantastic opportunity for a talented Global Regulatory Affairs Associate Director/ Manager.
Senior Clinical Project Manager, sponsor dedicated role, home based in Europe. CNS experience and...
IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for pati
Advanced Clinical is a global clinical development organization that provides CRO, FSP, Quality & Validation, and Strategic Resourcing services for...
CK Group are recruiting for a Senior Associate Regulatory Affairs to join a biopharmaceutical company at their site based in Uxbridge on a contract...
CK Group are recruiting for a Regulatory Affairs Senior Manager to join a biopharmaceutical company at their site based in Uxbridge on a contract b...
Senior Associate Regulatory Affairs12 Month Contract1.0 FTEUxbridge - UK Please note International relocations will not be considered for this role Jo
Senior Manager - Regulatory Affairs 12 Month Contract Applicants MUST be based in the UK already, you will not be considered should you wish to reloca
A fantastic new opportunity has been created to join a promising, US-headquartered life sciences organization, expanding across Europe. My client i...
Analytics - Healthcare - Pharmaceuticals - Data Strategy
Medical Device Regulatory Consultant Medical Device Regulatory Consultant This company is looking for a Medical Device Subject Matter Expert based ...
Full-time permanent opportunity for an experienced Hospital Account Manager to join our client in a UK wide role
The CSV Consultant will apply their knowledge and practical experience of CSV for laboratory (GMP) and ERP to validate systems including compliance fo
Regulatory Manager; Development & Strategy; Biopharma; Biologics & Pharma Products; Central/West London
UK based Pharmaceutical Manufacturer and R&D Laboratory seeks a Regulatory Affairs Manager.
Medical Writing Manager UK or US Home or Office At ICON, it's our people that set us apart. As a global provider of drug development solutions, our
Do you want to lead a team driving the progress of immunometabolism drugs? This one might be for you....
Want to develop your career in drug discovery working alongside industry experts? Take a look at this exciting new biotech company.....