Strong project management skills combined with a solid foundation of medical writing experience mean I can manage large or small projects, promptly producing high quality, accurate work.
I can quickly develop familiarity with your project, provide quotes on project timescales, and advise on the optimum way to present your data, key messages and outcomes.
I keep up to date with EMA and FDA requirements for investigational new drugs, new drug applications, and generic applications. I have experience with all clinical and non-clinical modules, as well as in a wide range of publications, medical communications and medical education projects.
I can therefore offer a full service approach, offering continuity and expertise across a drug life cycle, from bench to bedside.