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.
• 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.
• 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.
• 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.
• 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.
• 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.

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