CLINICAL TRIAL PROTOCOL WRITER jobs in LONDON, United Kingdom

, clinical discipline Substantial clinical study protocol experience, as lead author, required Experience leading and managing... Strong understanding of federal regulations, Good Clinical Practices, and ICH guidelines a plus Substantial clinical study protocol...

MMS

MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, including clinical trial transparency..., and ICH guidelines a plus Substantial clinical study protocol experience, as lead author, required Experience leading and managing...

MMS