I have over 15 years of experience in the following:

•Assists in preliminary study design, protocol, implementation, data reporting, and patient follow-up.
•Writes IRB protocol and consent forms; and other regulatory documents as required. Keeps current on regulatory requirements and ICH GCP guidelines.
•Researches and writes grants.
•Uses databases to generate reports, summarize data from clinical projects, and statistical analysis using SPSS. Assists with data interpretation.
•Writes and submits abstracts and manuscripts for conferences and publications.
•Manages budgets for the department.
•Performs data mining techniques to find ‘hot spots’ in patient care.
•Ensures research and administrative activities are compliant with Medicaid and FDA regulatory standards.
•Executes contracting requirements for consultants/ contractors.
•Develops and supports activities related to patient care, healthcare quality and outcomes measures.