Esomchi Ekeh

About Esomchi Ekeh

An Experienced Clinical Research Associate with a comprehensive understanding of clinical…

Experience

1. Snr Clinical Research Associate

   Rho

   Jan 2022 — Present · Houston, TX, US

   Contributes to the development of standard operating procedures (SOPs) for monitoring and quality control.•Conducts root cause analysis of data discrepancies, collaborating with data management teams for resolution.•Presents study progress updates and findings to sponsors and stakeholders during routine meetings.•Participates in vendor selection and management for central laboratory services and electronic data capture systems.•Collaborates with medical monitors to assess participant safety and manage adverse event reporting.•Coordinates with investigational sites to ensure timely and accurate completion of source data and CRF entries.•Provides guidance on protocol-specific procedures and ensured adherence to ICH-GCP guidelines.•Manages study budgets and timelines for global Phase trials, optimizing site performance and patient enrollment.•Mentors new CRAs in study procedures, data collection, and effective communication with investigative sites.•Identify protocol deviations and implement corrective actions, ensuring data integrity and participant safety.

Education

• Godfrey Okoye University

  Bachelor's degree

  2013