Azeez Bankole Email & Phone Number

Chicago, Il, Us

United States

• Completes onsite and remote monitoring activities in accordance with all ICH-GCP guidelines, applicableregulations, SOPs and study processes. Activities include qualifying potential investigative sites, initiatingclinical trials, maintaining study files, providing instructions to site personnel and study close out.• Verifies the protection of study participants by confirming informed consent procedures and protocolhave been performed in accordance to applicable… Show more • Completes onsite and remote monitoring activities in accordance with all ICH-GCP guidelines, applicableregulations, SOPs and study processes. Activities include qualifying potential investigative sites, initiatingclinical trials, maintaining study files, providing instructions to site personnel and study close out.• Verifies the protection of study participants by confirming informed consent procedures and protocolhave been performed in accordance to applicable regulations.• Ensures the integrity of clinical data and that the study is conducted in compliance with approvedprotocol, GCP, applicable regulations and SOPs.• Gathers and reviews information for assigned sites and identifies inconsistencies. With guidance fromproject and functional management, assesses risk and escalates as appropriate.• Writes and submits reports of investigational site findings and updates applicable tracking systems.Escalates observed deficiencies, issues, and corrective and preventative action plans as appropriate. Show less

Chicago, Illinois, United States

Akron, Ohio, United States

• Coordinating industry sponsored and federally funded clinical trials on prostate, lung, head & neck, colon, endometrial, and breast cancers.• Utilized various EDC systems such as EPIC, mosaiq, RedCAP, medidata, CTMS, iMedRIS.• Screen, consent, enroll, and assist in the overall clinical study coordination of cancer clinical trials.• Assist in identification and reporting of adverse and serious adverse events in accordance with specific protocol.• Prepared and processed all… Show more • Coordinating industry sponsored and federally funded clinical trials on prostate, lung, head & neck, colon, endometrial, and breast cancers.• Utilized various EDC systems such as EPIC, mosaiq, RedCAP, medidata, CTMS, iMedRIS.• Screen, consent, enroll, and assist in the overall clinical study coordination of cancer clinical trials.• Assist in identification and reporting of adverse and serious adverse events in accordance with specific protocol.• Prepared and processed all documentation through the Institutional Review Board (IRB), including submissions, continuing reviews, and amendments.• Communicating with hospital and research staff regarding patient care, status and protocol requirements. Show less

Akron, Ohio, United States

• Assisted with startup research utilizing zebrafish for determining personalized treatment plan in breast cancer patients.• Assisted with study design, methodology, collection and analyzation of data.• Drafted study consent and IRB application.

Kent, Ohio, United States

Parma, Ohio, United States

• Responding to various complaints within the county• Treating areas of standing water that may act as potential mosquito breeding site• Conduct mosquito surveillance (trapping) to monitor the population and potential disease activity withinthe different nearby cities

Master'S Degree, Clinical Epidemiology

Bachelor'S Degree, Clinical Trials Research