£40,000 - £59,999 Full Time Permanent jobs in London (Greater)
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Found 10 Direct Employer jobs
THE COMPANY PHASTAR is a multiple award-winning, data focused CRO specialising in providing statistics, programming, data management and data scien...
We have an exciting opportunity for a medical writer/senior medical writer who loves to develop publications based on HEOR data.
Are you a skilled regulatory expert looking to help us bring forward the day when all cancers are cured? This exciting new role sits within...
Manager of Regulatory Strategy Award Winning PRA and our employees have won numerous awards and accolades in the CRO industry and 2020 hasn’t been ...
Senior Regulatory Labelling Manager Home or office based in UK/US COVID PRA has been contributing to the battle against COVID since day 1 and whils...
Statistical Programmer, SAS Programmer, CDISC, SDTM, ADaM, Clinical Trials, PK/PD data, Data Analysis
Clinical Pharmacology Scientist, Medical Writing, Regulatory Writing, Study Protocol, Study Report, Informed Consent, Ethics Submission
In this central role, you will be responsible for supporting CDMS Programming activities as related to building study databases, system reports in DM.
The point of contact for day to day activity on a study with key responsibilities for study set-up and close-out tasks in DM team
German speaking CRA to be based in the UK and remotely manage an infectious disease study, as well as UK sites for oncology programme