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| Desired Industry: Biotech |
SpiderID: 17610 |
| Desired Job Location: Charlotte, North Carolina |
Date Posted: 12/8/2007 |
| Type of Position: Full-Time Permanent |
Availability Date: |
| Desired Wage: |
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U.S. Work Authorization: Yes |
| Job Level: New Grad/Entry Level |
Willing to Travel: Yes, 50-75% |
| Highest Degree Attained: Bachelors |
Willing to Relocate: No |
Objective:
To begin a challenging career in clinical research using my education and 30plus years of clinical experience as a strong base.
Experience:
Dawn L. Golladay MLT(ASCP)
1007 Astoria Drive
Monroe, NC 28110
(704) 578-3716
dawngolladay@yahoo.com
SUMMARY
• Bachelor of Arts in Healthcare Administration
• Completion of Clinical Research Associate training program
• Procedure writing and medical staff training experience
• 25 years medical laboratory experience, in various settings
• Oversaw daily laboratory operations and CLIA inspections.
• Evaluated and maintained quality control programs.
• Clinical Skills: EKG, phlebotomy and chain of custody collections.
• Exceptional skills in organization, attention to detail, time
management and prioritizing tasks.
• Available to travel within United States
PROFESSIONAL TRAINING
Clinical Research Associate Education and Training Program Conducted by Medical Research Management, Inc.
“Fundamentals of Clinical Research” June, 2003
140 hour Training program included the following topics
• The drug research and development process, identifying and reporting of non-serious and serious adverse events, principles of data management and query resolution, protocol development, case report form design and informed consent writing.
• Good clinical practices 21CFR 312 IND, 21 CFR 50 Protection of Human Subjects, 21CFR 56 IRB, and 45 CFR 46, 21 CFR 54 Financial Disclosure by Clinical Investigators. International conference on Harmonization (E6) GCP Consolidated guideline and (E2A) Clinical Safety Data Management.
• Monitoring method and responsibilities: Systematic approach to monitoring, managing essential documents and clinical trial materials. Selecting investigators and conducting pre-evaluation, study initiation, interim and close out visits. Writing pre-visit letter, follow up letter and site visit reports. Performed five mock site visits utilizing case studies.
Criteria for Course Completion: Comprehensive course examination, ICH/GCP regulatory examination, and performing a site monitoring visit identifying 80% of the deficiencies.
EDUCATION
Bachelor of Arts in Healthcare Administration July, 1999
Concordia University Wisconsin, Mequon, Wisconsin
Associate of Applied Science in Medical Technology May, 1979
Sauk Valley College, Dixon, Illinois
PROFESSIONAL EXPERIENCE
Quest Diagnostics, Inc., Las Vegas, Nevada
Medical Laboratory Technician November2000-present
Responsible for the daily oversight of 1500 (or more) patient specimens, machine maintenance, quality control procedures and recordkeeping within the blood culture section of the microbiology department. Also new culture setup and reporting critical value results to clients via telephone and computer entry.
University of Illinois, College of Medicine, Rockford, Illinois
Medical Laboratory Technician May 1988-October2000
Laboratory generalist responsible for laboratory operations, patient specimen collection and testing, evaluating/solving problems related to laboratory operations, patient care, testing and billing issues. Experienced in the areas of chemistry, urinalysis, hematology, and coagulation.
Candidate Contact Information:
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