Senior Regulatory Writer ''A''

Senior Regulatory Writer

At least 5-8 years of regulatory writing experience (clinical study reports, investigator brochures, protocols (phase 1-4), periodic safety update reports, etc.) 
Advanced knowledge of clinical research processes and drug development, as well as ICH, GCP, and other such industry guidelines 
Experience across document types and therapeutic areas/diseases/drug classes 
Ability to understand and interpret complex clinical trial data 
Clear, concise scientific style of writing with a high level of attention to detail 
Prior experience writing entire regulatory documents 
Good written and oral English language skills 
Ability to work under tight timelines and manage multiple tasks.
                                                                                

For more info click on mentioned link