Summary Study Coordinator with 6 years' experience specializing in technical support of animal studies requiring GLP compliant interpretations, analysis, documentation, and reporting of results per FDA regulations beginning with protocol development support and creation of shell reports resulting in a Final product ready for FDA Regulatory Filings. Areas of Expertise / Core Competencies * Highly dependable, focused and determined team player with proven analytical skills, ability to pay attention to details and adept at conducting up to five to six simultaneous research studies. * Fifteen years' experience in the Biomedical field. * Improved presentation of study data and reports by effectively reviewing documents and ensuring a high level of accuracy, quality and consistency. * Facilitated the operation of studies by acting as liaison between the Study Director, sponsor, client, and sub-contractors to help coordinate study operation and documentation. * Possesses excellent organization skills demonstrating systematic expertise in obtaining and using information resulting in meeting all study closure deadlines in my six years as study coordinator.

Highlights:

• Documentation
• Good Laboratory Practices
• Protocol
• Analytical Skills
• Biomedical Industry
• Quality
• Quality Assurance
• Coordinator
• Medical Devices
• Regulatory