Jovia Adu
Clinical Research Trainee @Clinical Research Fastrack
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WORK HISTORY
Clinical Research Trainee @Clinical Research Fastrack
US
ICH GCP E6 R (3) FDA Regulations 21CFR 11, 50, 54, 56 and the Common Rule 45CFR46 Data Management Informed Consent ProcessClinical Trial Operations from feasibility through close-outGDP following ALCOA-C principles Identification and reporting of AEs and SAEsQuality Assurance, Monitoring and Query Resolution Comprehension and Execution of Clinical Trial Protocols Maintaining a regulatory binder, housing essential documents including but not limited to 1572, DOA, Training Logs and other Investigator Site File (ISF) documents
ABOUT JOVIA ADU
Certified Clinical Research Professional with extensive expertise in ICH/GCP guidelines…
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