QUALIFICATION SUMMARY
Strong background in biomedical science and translational research.
Extensive experience in scientific and medical writing/editing; being author, co-author and editor of numerous papers, abstracts, conference presentations, research grant, and clinical and regulatory documents.
Experience in clinical study data analysis, IRB application and literature search; knowledge of current FDA regulations, EMEA and GCP/GLP/GMP guidelines; systemic training in regulation, clinical trial design and implementation, biostatistics, and comprehension of drug development.
Experience in the use of a variety of scientific software packages of reference management, graph and data analysis.
Excellent communication skills to deliver complex concepts to lay audiences and experts; ability to coherently organize material for others with a focus on attention to details.
Strong initiative and desire to learn. 

PROFESSIONAL EXPERIENCE 
Senior medical writer: inVentiv Health Clinical, APAC                                   2014.02 – Present
   Manage medical writing projects according ...