Kiara S. Brown
Research Associate Ii @Atrium Health
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WORK HISTORY
Research Associate Ii @Atrium Health
Charlotte, NC, US
Division of Gastrointestinal and Minimally Invasive SurgeryAwards:Living Our Commitments NominationPresentations:Scarola GT, Wilson HH, Ku D, Brown K, Tawkaliyar R, Colavita PD, Augenstein VA, Heniford BT. Creating the Infrastructure to Make Hernia Research a Reality. European Hernia Society, May 2023, Barcelona, Spain, Best Oral-3rd PlaceMarturano MN, Ayuso SA, Elhage SA, Tawkaliyar R, Brown K, Ku D, Fischer JP, Heniford BT, Augenstein VA. Increasing Body Mass Index Escalates Surgical Sute Occurances with Panniculectomy during Abdominal Wall Reconstruction. ASPS Plastic Surgery the Meeting. Boston, MA. October 2022.Marturano MN, Ayuso SA, Aladegbami B, Tawkaliyar R, Brown K, Augenstein VA, Heniford BT. Component Seperation Techniques following Failed CST in Re-operative Massive Ventral Hernias. ASPS Plastic Surgery the Meeting. Boston, MA. October 2022.Publications:“Observational Study of Complex Abdominal Wall Reconstruction using Porcine Dermal Matrix: How Have Outcomes Changed Over 14 Years?” Surgery Journal, May 2022 (See Publication Section.)Scarola GT, Wilson HH, Ku D, Brown K, Tawkaliyar R, Colavita PD, Augenstein VA, Heniford BT. Creating the Infrastructure to Make Hernia Research a Reality. Accepted to the European Hernia Society, May 2023
EDUCATION
Winthrop University
B.A in Psychology, Gerontology
The Johns Hopkins University
Online Course, Fundamental Neuroscience of Neuroimaging
Stanford University
Online Course, Writing in the Sciences
Johns Hopkins Bloomberg School of Public Health
Online Course, Design and Interpretation of Clinical Trials
Spring Valley High School
High School Diploma
University of Pennsylvania
Graduate Certificate, Neuroscience
ABOUT KIARA S. BROWN
I have received intensive training from trained clinical research professionals: ICH GCP E6 R2, 21CFR (11, 50, 54 + 56), FDA Regulations, IRB, ALCOA-C principles, regulatory affairs, maintaining regulatory binders and essential documents, feasibility through close out, clinical trial budgeting, following a protocol, data quality assurance, reporting adverse events, protocol deviations and violations, investigator responsibilities, recruitment and retention of research subjects, monitoring quality assurance, data management systems, clinical trial operations, informed consent process, and research skills. I am excited to join an industry dedicated to the advancement of treatments and medicine to combat diseases and disorders; and restore health. I am particularly interested in neurodegenerative diseases - Parkinson’s, Huntington’s, and Alzheimer’s.
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