Occupation:Clinical Research |
Location:Saint Petersburg, FL |
Education Level:Master |
Will Relocate:YES |
Description
Summary of Experience Proficient Clinical Research Professional with strong interpersonal skills and expansive knowledge of medical terminology. As an active part of a clinical research team, I am knowledgeable of GCP, ICH, IATA, HIPAA and other relevant Regulatory Guidelines. Experience includes working with multiple clinical trials in various therapeutic areas. This has also led to obtaining a widespread knowledge base of clinical trial process including: pre-initiation, contract review & implementation, initiation, and closeout. Proven experience in research coordination, regulatory affairs, data management, and project administration. Technical skills include extensive knowledge of Microsoft Office, various IRB & EDC Systems. Seeking longevity within a company focusing on medical research where my key professional experiences can be transferred and built upon within these areas: � Research Coordinator � Project Management � Biological/Laboratory Experience � Regulatory Affairs Experience � Data Management/Quality Assurance � AE Reporting � Report & Chart Generation � Knowledgeable of Medical Terminology
Work Experience
| COMPANY | POSITION HELD | DATES WORKED |
|---|---|---|
| (Confidential) | Clinical Research & Regulatory Coordinator | / - Present |
| (Confidential) | Clinical Research Data Coordinator | / - Present |
| (Confidential) | Coastal Training Specialist | / - Present |
| (Confidential) | Recreation Programmer | / - Present |
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