Kayode (Kay) Adebayo

Clinical research is an important aspect of bringing smiles to people's faces. Watching their back when they are even fast asleep.Contributing my quota in any way possible to this laudable goal of FDA, ICH-GCP in areas of subjects' safety, accurate and complete data and carrying out drug and device trials within the approved frameworks of local and international laws and regulations is always my pleasure.Specialties: Mastery of clinical research monitoring and regulatory affairs .Proficient in Microsoft word,Excel,power point and SPSSEDC: Exposure to Medidata and Open ClinicaRobust medical background (an MD), experimental & clinical laboratory practice, Clinical Pharmacology management and University lectureship in the College of Medicine experience.Specialties: Knowledge of Clinical research monitoring:Pre-study site selectionSite initiation visitRoutine site monitoringClose out visitSAEs detection and reconciliationRegulatory reconciliationDrug/study product accountability or reconciliationVerification of site compliance with protocolVerification of site compliance with ICH-GCPSOPs writingInformed consent writingProtocol writing and expatiationSubject recruitment and retentionClinical trial monitoring.Scientific writing and presentation.Conflict resolutionGood Clinical Practice (GCP)Good Laboratory Practice (GLP)Scientific Reviews Multitasking THERAPEUTIC AREAS: Knowledgeable [based on robust medical background] in the following areas:•Cardiovascular, Renal (Nephrology), Neurology, Infectious diseases, Respiratory, GI, Musculoskeletal, Obstetrics & Gynecology and neurology.