Chukwunonso Livinus Udeh
Consultant Clinical Research Associate
- Department:Clinical Research/Public Health
- University:Clinique Research Development Limited
- Country:Lagos, Nigeria
Chukwunonso Livinus Udeh is a Clinical Research professional with about 5 years of knowledge/skills/experience in animal experimentation, public health interventions, and world-class clinical trials. He has actively participated in the planning, conduct, and monitoring of phase I, II, III, pharmacovigilance studies ranging from Vaccines, Oncology, RA and Cardiology. His ultimate goal is to tackle those ethical issues revolving around drugs, medical devices, nutraceuticals, cosmetics and vaccines development, in order to address specific health needs ranging from Nigerian to African and the World at large.
Experience in Clinical Research/Public Health with end to end monitoring experience in India and West Africa for Surveys, Phase I, II, III studies, and Pharmacovigilance. This includes a year’s experience working as an M&E volunteer in Nigeria for an HIV/AIDS study.
PROFESSIONAL EXPERIENCE Consultant Clinical Research Associate August 2018 till date: Likak Research, Dakar, Senegal February 2019 till date: Margan Clinical Research Organization, Accra, Ghana November 2019 till date: Clinique Research Development Limited, Lagos, Nigeria Activities performed include; ? Examined the overall conduct of the study ? Monitored the survey live data capture on ODK in the field ? Assisted the team in the preparation of Investigator Site File ? Performed paper source data verification ? Verified adherence of the data collection process to GCP and Protocol ?
Reviewed Informed consent documentation to ensure that subjects’ rights are protected ? Conducted short training for the study team to maximize compliance ? Reviewed the survey database and electronic data capture for completeness and accuracy ? Documented Monitoring visit with a report according to the Sponsor’s SOP ? Prepared a follow-up letter sent to the Principal Investigator.
Activities performed under the under the Strengthening Integrated Delivery of HIV/AIDS Services (SIDHAS) project include;
- Entered and updated HIV patients’ data into DHIS and LAMIS database.
- Assisted in quarterly retention and audit determination (RADET).
- Collected and updated monthly reports from facilities using Pre-ART, ART, PMTCT registers, etc.
- Brought to the attention and knowledge of the M&E team, issues that needed to be resolved such as data inconsistencies, missing data, outliers, etc.
Clinical Research,Public Health, Pharmacology, Oncology, Biomedical Sciences
Clinical Research, Regulatory Affairs, GCP, GCLP, GLP, GMP, Quality Control, Quality Assurance, Monitoring/Evaluation, Auditing, Informed Consent process, AE/SAE reporting, Project Management, Medical Writing, Pharmacovigilance.