Reviewed data for trends, patterns, and causal analysis.Conducted advanced qualitative and quantitative data analysis; interprets and evaluates results; prepares reports and/or presentations; monitors and collects research data to assess accuracy, validity, and integrity

Reports, monitors, distributes and maintains files for all safety information including Investigational Drug Brochures, IND safety reports and Serious Adverse Events (SAE) reports.
Assist researchers to design studies that may show the seriousness of a disease, predict a specific disease's seriousness, evaluate a new treatment, assess the safety and effectiveness of medications and increase knowledge of environmental issues. Managed study start-up activities (input in protocol development, development of Informed Consent Forms, Case Report Forms, and related study material).Developed and implemented innovative approaches for site recruitment, selection and initiation activities. Conducted periodic clinical site monitoring visits to ensure the integrity of clinical data and to ensure proper storage, dispensation and accountability of clinical trial materials, according to applicable regulatory, protocol, and company guidelines.

Analyzed substance abuse trends and patterns and developed, implemented, and evaluated substance abuse prevention programs.

Master of Public Health specializing in Epidemiology/ Statistics

Bachelor of Science specializing in Health Science/ Community Health