Funke Odumade

About Funke Odumade

I manage complex Phase clinical trials — and I make them run better. With…

Experience

1. Senior Clinical Research Coordinator

   IQVIA

   Jul 2024 — Present

   Providing clinical research support to investigators to prepare for and execute assigned research studies, including: review study protocols, Case Report Forms (CRFs), other study-specific documents, and electronic data capture systems used to record clinical research data* Collect and submit regulatory/ethics documentation as required by relevant regulatory bodies governing the conduct of clinical research* Recruit and screen patients for clinical trials and maintain subject screening logs* Design and maintain source documentation based on protocol requirements* Schedule and execute study visits and perform study procedures* Collect, record and maintain research subject study data according to study protocol and SOPs, preserving quality control for content, accuracy and completeness* Monitor subject safety and report adverse reactions to appropriate medical personnel* Correspond with research subjects and troubleshoot study-related questions or issues* Assist with study data quality checking and query resolution* Perform a variety of complex clinical research procedures including but not limited to ECG, sample collection, spirometry, vital signs, dose verification, cannulation and cardiac telemetry monitoring* Record, report and interpret study findings appropriately to develop a study-specific database* Assist investigator in verifying that research study objectives are met on time, within budget and according to applicable protocol requirements, clinical research regulations and quality standards* Assist in maintaining adherence to investigator site staff training requirements by auditing and maintaining training records* Prepare for and attend study monitoring visits, study audits, and regulatory inspections with clinical research regulatory agencies.