Back to jobsStrong verbal and written communications skills coupled with general knowledge of FDA and ICH rules, regulations and guidelines governing conduct of clinical studies and regulatory documents
Detail-oriented, with good organizational, prioritization, and time management proficiencies; proactive approach.
Ability to work cross-functionally
Advanced computer software experience (including but not limited to MS Word, Excel, PowerPoint)
Ability to interpret and present scientific and clinical trial data and understand statistical methods and analysis plans.
Proven ability to facilitate issue/comment resolution as it relates to finalization of medical writing deliverables.