Izzy Obasuyi Email & Phone Number

United States

Senior Clinical Research Associate, Worldwide Clinical Trials04/2021 to Current•Expertly executed the coordination and monitoring of site monitoring tasks and activities, ensuring optimal efficiency and timely completion of all necessary work•Provided comprehensive and highly effective support to study site personnel, delivering technical and scientific guidance to ensure accurate interpretation and exchange of scientific information throughout all clinical trials•Successfully oversaw all aspects of qualification, site initiation, interim, and close-out monitoring visits, ensuring strict adherence to monitoring plans, protocols, and regulations, and maintaining the highest levels of quality and compliance•Monitored and ensured sites' compliance with study protocols, identifying and addressing any issues promptly

United States

•Elaborately created, thoroughly reviewed, and consistently maintained monitoring standard operating procedures and monitoring tools, encompassing monitoring plans, monitoring reports, and corrective and preventive action plans, to maximize the efficiency and precision of conducting monitoring tasks•Dedicatedly developed and meticulously maintained strong site relationships, thereby fostering seamless continuity throughout all phases of the trial and establishing an exceptional collaborative rapport with site personnel•Ensured unwavering compliance with the clinical trial protocol by diligently conducting on-site visits, rigorously reviewing case report forms (CRFs), and maintaining constant communication with clinical research coordinators•Conducted pre-study visits to evaluate the suitability of investigational sites for the investigation study, ensuring the availability of required facilities, resources, and qualified personnel

United States

•Identified potential issues with conducted trials, protected study topics, ensured data integrity, and provided retraining to site staff as necessary•Provided detailed preparation and instructions to designated site staff for conducting analysis in full compliance with relevant guidelines, SOPs, and regulations•Delivered ongoing training to test site staff on proper trial conduct when required•Ordered and meticulously maintained research records, including consent forms, registries, and patient charts

United States

•Created and presented routine reports on critical study parameters such as patient screening, eligibility, enrollment, and retention, providing valuable insights to the study team and sponsor•Maintained effective communication with the study team and sponsor, ensuring that all required information was conveyed accurately and in a timely manner•Facilitated the informed consent process, monitored adverse events, and reported them according to protocol guidelines, ensuring patient safety and data quality•Assisted with research-related fundraising events and publications, contributing to the success of fundraising campaigns and enhancing the visibility of the study•Managed the processing and shipment of study specimens, including blood, urine, and CSF samples, using various software platforms such as eClinical, Siebel, VeevaVault, Medidata Rave, Inform 6.1, Trialmaster, Datalabs, and IWRS (Endpoint, Clinphone, and Suvoda), ensuring the integrity of study data and adherence to protocol requirements

Nigeria

•Analyzed various types of patient samples such as blood, body fluids, and urine to aid in the diagnosis•Managed the collection of 50-100 samples daily, including labelling, and record-keeping•Ensured adherence to quality and safety procedures throughout testing processes•Evaluated and utilized 2-3 automated testing devices, such as spectrophotometry, colourimetry, and mass spectrometry, to expedite diagnosis