Experienced and highly qualified Clinical Research Associate with over 10 years of experience in researching and knowledge of study startup, monitoring, and regulatory processes in the Pharmaceutical Industry. Highly proficient in performing quality assurance control on laboratory best practices while leveraging R&D experience to consistently achieve goals. Extremely focused and results-oriented in supporting complex, deadline-driven operations with a strong ability to identify goals and resolve complex issues during initial stages. Currently pursuing a manager role which will effectively utilize all skills, abilities, and areas of expertise as follows: Key Strengths Team Leadership Research & Development Project Management Supply Procurement Document Review Report Generation Laboratory Operations Process Improvement Technical Writing Data Collection/Analysis Medical Terminology Quality Assurance Control Scientific Evaluation Team Collaboration Conducting Experiments Phase I-IV Trials

Highlights:

• Data Management
• Documentation
• Management
• Systems Administrator
• Clinical Research
• Health Insurance Portability And Accountability Act
• Research
• Project Management
• Project Manager
• Protocol