Jyke Ibeh
Clinical Research Professional @Clinical Research Fastrack
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WORK HISTORY
Clinical Research Professional @Clinical Research Fastrack
ICH GCP/Protection of Patient rights2. FDA Regulations 21 CFR Parts 11, 50, 54, 563. Data Management systems, Electronic Data Capture (EDC)4. Informed Consent Processes5, Good Documentation Practices (GDP) following ALCOA-C principles6. Clinical Trial Operations from Feasibility through close - out7. Identification, documentation and reporting of AEs and SAEs8. Quality Assurance, Monitoring and Query Resolution9. Comprehension and execution of Clinical Trial Protocol10. Maintaining Regulatory Binder housing essential documents including, but not limited to Form 1572, Source Documents, TMF, DOA log, Training logs, ICF, Financial Disclosure Forms, Case Report Forms, Investigational Brochure, SOPs, Curriculum Vitae, Site Visit Logs, Correspondences, Trial Master Files (TMF) and other Investigator Site Files (ISF) Documents.
EDUCATION
University of Ibadan
Bachelor's degree, Physiotherapy
Lund University
Master of Public Health, MPH
Mercer County Community College
Associate's degree
Malmö University
Master of Arts - MA, Leadership & Organization
ABOUT JYKE IBEH
Passionate and goal oriented Public health expert with background in Clinical research, Project management and Physical Therapy. Sound knowledge of Clinical trials in accordance with ICH GCP guidelines. Skilled in health promotion, rehabilitation, clinical research education, quality assurance and improvement.Resilient and obsessed with clinical research, dependable team player, and willingness to learn new things
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