Member Profile
Kecia Brown
I am knowledgeable about a number of regulatory guidelines and several style manuals. My writing and editing experience includes abstracts, book chapters, educational assessments, grants, journal articles, slide presentations, and posters. As a participant in public health project evaluation and implementation, I have written surveys and health information materials for the lay person. As a consultant clinical writer, I have participated in the preparation of regulatory documents for U.S. FDA and European Agency for the Evaluation of Medicinal Products (EMA) submission. I have written manuals for device operation, market research reports, standard operation procedures (SOPs), and white papers. I have covered meetings for the following U.S. agencies: NCI, NIMH, NIAID, and AHRQ. I have written the scientific sections for RFPs and I have summarized expert panel responses on grant reviews.
Home phone: 2022039779
Email: kecia.brown@gmail.com
Years in the field: 24
Years freelancing: 3
Kecia Brown
I am knowledgeable about a number of regulatory guidelines and several style manuals. My writing and editing experience includes abstracts, book chapters, educational assessments, grants, journal articles, slide presentations, and posters. As a participant in public health project evaluation and implementation, I have written surveys and health information materials for the lay person. As a consultant clinical writer, I have participated in the preparation of regulatory documents for U.S. FDA and European Agency for the Evaluation of Medicinal Products (EMA) submission. I have written manuals for device operation, market research reports, standard operation procedures (SOPs), and white papers. I have covered meetings for the following U.S. agencies: NCI, NIMH, NIAID, and AHRQ. I have written the scientific sections for RFPs and I have summarized expert panel responses on grant reviews.