Kehinde Ogunremi
Clinical Research Professional
- Role
- Clinical Research Coordinator at Southwest Family Medicine Associates
- Location
- Dallas-Fort Worth, TX, US
- LinkedIn followers
- 500 followers
About Kehinde Ogunremi
I am a trained Clinical Research Professional with extensive experience in the informed…
Experience
Clinical Research Coordinator
Southwest Family Medicine Associates
Jan 2024 — Present · Dallas, TX, US
Establish and maintain investigator site file in inspection ready state, by ensuring ongoing completeness and filling of study regulatory documents. • Prepare and submit documents required for regulatory ethics committees review including initial IRB and RDC approval, contingencies response, annual continuing review, protocol amendments, study close out, and adverse event reporting. • Draft informed consent forms in compliance with local IRB policy and 21 CFR 50, design research source documents and review medical records for pre-screening activities. • Review informed consent documentation to ensure compliance with 21 CFR 50, review inclusion/exclusion criteria to confirm participant eligibility, and assure timely documentation of protocol deviations.
Education
Owens Community College
Associate's degree, Business Studies
2015 — 2017
University of Toledo
Bachelor of Business Administration - BBA, Information Systems
2018 — 2019
Clinical Research Fastrack
Clinical Research Professional
VIARES Clinical Research Associate Training Course
Bachelor of Science - BS, Information Systems
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