Clinical Research Consultant

• Apr 2020 - Present

Clinical Research Associate II

• Sep 2019 - May 2020

Reviewing data and source documentation from investigational sites for accuracy and completeness· Ensuring adverse events and protocol deviations are reported in an efficient manner· Ensuring that device complaints and malfunctions are reported according to Abbott Policies and Procedures· Resolving and/or facilitating resolution of problems including identification of cause and actions to prevent re-occurrence Reviewing data and source documentation from investigational sites for accuracy and completeness· Ensuring adverse events and protocol deviations are reported in an efficient manner· Ensuring that device complaints and malfunctions are reported according to Abbott Policies and Procedures· Resolving and/or facilitating resolution of problems including identification of cause and actions to prevent re-occurrence

Clinical Research Associate

• May 2016 - Sep 2019

• Monitor activities at clinical study sites to ensure adherence to Good Clinical Practice (GCP) guidelines, SOPs, and study protocols.• Review of site regulatory documents maintained in the investigative site file (ISF).• Preparing and disseminating site visit confirmation letters, visit reports and follow up documentation in a timely manner.• Conducts clinical trial feasibility for site selection.• Participate in the study development and start-up process including reviewing protocols, designing and/or reviewing CRFs, preparing Informed Consent forms, developing study documents, organizing and presenting at investigator meetings, working with management on monitoring strategy, and/or developing project-specific CRA training. • Responsible for all aspects of study site monitoring including routine monitoring, close out visit, conducting pre-study and initiation visits as outlined in the Clinical Monitoring Plan (CMP), applicable SOPs and regulatory guidelines.• Working as an integral study team member with respect to quality, integrity of the data timelines, and cost effectiveness while monitoring.• Assist the investigational site in the management of timely query resolution.• Assist in clinical trial disclosure ensuring full regulatory compliance. • Assist project teams by ensuring that all data is collected and submitted within appropriate timelines and communicates these timelines to the investigational sites.• Coordinate and generate reports as required and handled multiple project as well as perform a variety of complicated tasks such IVRS data verification for drug accountability.

Clinical Research Assistant

• Mar 2013 - Jun 2015

• Developed and wrote protocols; located and accessed the feasibility of sites.• Conducted semi-structured interviews with stakeholders and community leaders to identify health needs in the disadvantaged communities in London.• Developed questionnaires, and collected and analyzed data for the `Well-London` projects used in monitoring and evaluating project effectiveness.• Provided training programs for community volunteers and other health professionals.• Part of the supervisory team that conducted a Randomized Control Trial (RCT) in compliance with the UK Medicine & Healthcare Products regulatory Agency (MHRA) requirements. This RCT was used to evaluate the effectiveness of the `Well London projects`.

Medical Intern

• Jan 2011 - Feb 2012

• Completed post-medical school clinical internship required to be a fully certified medical doctor in Nigeria.• Rotated through various departments such as Internal Medicine- Nephrology, Surgery, Obstetrics&Gynaecology, Pediatric Neuro, and Psychiatry. • Completed post-medical school clinical internship required to be a fully certified medical doctor in Nigeria.• Rotated through various departments such as Internal Medicine- Nephrology, Surgery, Obstetrics&Gynaecology, Pediatric Neuro, and Psychiatry.