- Los Angeles US-CA
- [email protected]
Over 10 years experience as a writer, editor and consultant on medical articles, scientific manuscripts, and regulatory documentation directed at physicians, pharmaceutical/biotech and regulatory agencies. Possess extensive experience in both publications and regulatory drug development documents. Broad understanding of scientific/medical concepts and the ability to write to a physician or layman audience, while providing quick turnaround with error-free copy. Therapeutic areas with particular expertise: rheumatoid arthritis, cardiovascular disease, oncology, diabetes, tuberculosis, HIV, and schizophrenia/bipolar disorder. Exceptionally strong literature research skills. Professional Summary: ♦ Possess in-depth knowledge of the pharmaceutical research industry and regulatory guidelines in the US and the EU (ICH, FDA, GCP, GxP). Possess IRB certification. ♦ Ability to write, edit, and proofread accurately and efficiently. ♦ Organized, meticulous editor, resourceful, creative and efficient writer. ♦ Well-versed competency in critically analyzing clinical data and distilling complex concepts into language suitable for a variety of medical audiences. ♦ Experienced in re-writing and substantive, developmental and English review editing of manuscripts submitted for publication to US journals.