CLINICAL TRIAL PROTOCOL WRITER jobs in EUROPE ENGLAND, United Kingdom

and scientific innovation for generations to come. The role: We are seeking an experienced Clinical Trial Protocol Writer... teams to develop clinical trial protocols. Conduct literature reviews and research to support protocol development...

, 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 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...

of a program. Assures that clinical trial objectives of each study fit with the clinical program strategy. Ensure that documents.../IECs Provides medical input into country feasibility. Support study team Has oversight of clinical input to protocol...

to meet the stated objectives. Assures that clinical trial objectives fit with the clinical program strategy. Ensure... to protocol/study team for monitoring guidelines, statistics analysis plans, ICDs, clinical review forms, data edit checks, data...

to and refine templates for clinical trial documents, eg protocols, IBs, ICFs, CSRs, etc. May provide support... Life Sciences Solid experience as a medical writer preparing clinical/regulatory documents in the pharmaceutical...