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Online Resumes with "IRB documents"
6 Years Experience in NIH funded clinical trial and research
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.
Tags for this Online Resume: Public health Research experience, Clinical trial experience, Regulatory (IRB) documents., MS office and SPSS, ArcGIS and geodatabases
Clinical Research Coordinator
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 Coordinator, Recruitment, Statistics, Certified, Data analysis, IRB documentation
Lead Clinical Research Coordinator - 4+ Years of Experience - Near 48304
Tags for this Online Resume: SPSS, CCRP, IRB documents, Multicenter Clinical Trials, SAE reporting, Data management, internal monitoring, GCP and FDA regulations
Clinical Regional Monitoring - 18 Years of Experience - Near 08053
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
Clinical Research
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...
Tags for this Online Resume: Chemotherapy, Clinical Research, Collection, Gastrointestinal, Oncology, PEDIATRIC, Protocol, Support
