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Online Resumes with "IRB documentation"
To utilize my academic qualifications and professional experience to contribute to the wellbeing of the community/society and thus to the enhancement of public health field.
Submit IRB documentation. Recruitment and screening. Medical examination. Conduct the study. Data analysis. All tables and reports from the study.
Tags for this Online Resume: Clinical Research, monitoring, Cancer, Prestudy, initiation and close out visits, Inflammatory Diseases, Cardiovascular, regulatory review, Good Clinical Practices, New Jersey, Phase I - III Clinical trials, EDC, drug accountability, infectious diseases, laboratory and study supply, IRB documentation
PROFESSIONAL SUMMARY: Experienced Clinical Research Professional seeking career advancement with a CRO where I can make a positive contribution by utilizing my clinical research expertise. In-depth knowledge of clinical trial policies and procedures, study protocols, GCP guidelines, ICH guidelines, regulatory clinical trial documentation requirements, IRB documents submittal, sponsor electronic data capture systems for data...