Ying He, Md, Mph Email & Phone Number

Atlanta, Georgia, United States

Atlanta, Georgia

Identify the needs of people living with HIV/AIDS of and assess the service gap in current system of delivery primary care and supportive service in the 20 Atlanta counties EMA (Eligible Metro Area) . Plan, motoring, and oversee the evaluation activities on data collection, analysis, interpretation, and dissemination. Track the implementation of comprehensive plan through collaboration with internal and external partners to address priority issues.

Jackson, Mississippi

State occupational health surveillance program: data analysis for identification and tracking of occupational health risks/exposures, and health effects in an effort to increase understanding of how the workplace impacts the health and lives of Mississippi's workforce.

Jackson, Ms

• Developed research strategies and conducted epidemiologic research in obesity, STI/ HIV, teen pregnancy prevention. Provided support including protocol development, literature reviews, manuscript development, project management, and data analysis (primary and secondary data including EMR, BRFSS, survey data)• Established up-to-date work plans and performance measures for projects to promote viable implementation procedures. • Conducted site visits and fidelity monitoring of on-going projects among sub-grantees.• Presented findings to a variety of audience (scientific professionals, stakeholders, and general public) at local, regional, and national conferences.

Wuhan, Hubei, China

• Assessment of epidemiological data and literature review relevant to safety issues by using various publicly available sources (i.e., historical data, electronic health record [EHR] data, disease registries, census data).• Monitored active database of adverse drug/medical devices events in Hubei Province, China and provided safety updates (PSUR) to China FDA periodically.• Ensured post market surveillance activities were complied with FDA requirements and applicable regulations.• Provided scientific regulatory expertise pertaining to medical products with emphasis on safety.

Wuhan, Hubei, China

• Ensured consistency of research outcomes and facilitated multiple rounds of review and revision of documents.• Enforced Standard Operating Procedure (SOP) during the entire process of drug research to meet the standard of Good Laboratory Practice (GLP).• Evaluated, initiated, and managed protocol amendments, safety reports, and correspondences with FDA regarding regulatory applications and submissions for the medical products.

Conducted research to support new drug application specialized in toxicology studies of new drug.• Produced high quality technical reports and publications in the area of pre-clinical drugs safety evaluation.• Developed the toxicology section of drug applications or related regulatory documents for FDA, where details on safety are required.

Master'S Degree, Public Health

Activities and Societies: 2014-2015 academic year scholarship award by JSUSummer obesity research training program ,2014 Poster.

Summer Session In Epidemiology (Sse), Clinical Trial

Master'S Degree, Pharmacology

Medical Degree, Medicine