Obinna A

About Obinna A

I am a dynamic and results-oriented Clinical Research Associate with a continuous track…

Experience

1. Senior Clinical Research Associate

   Vyaire Medical

   Jan 2023 — Present

   Facilitated site initiation visits for the purpose of training site personnel on the protocol, study procedures, patient recruitment and retention requirements, case report forms, completion and retention requirements, adverse events, reporting procedures, and overall management. Manage all aspects of clinical trials, including protocol development, site selection, initiation, monitoring, and close-out activities.Conduct pre-study, initiation, interim, and close-out site visits to ensure compliance with protocol, regulatory requirements, SOPs, and ICH-GCP guidelines.Perform source data verification, review case report forms (CRFs), and resolve data discrepancies in a timely manner.To facilitate smooth trial conduct, develop and maintain strong relationships with investigational sites, study coordinators, and other key stakeholders.Provide training and support to site staff on protocol requirements, study procedures, and regulatory compliance.Coordinate with cross-functional teams, including clinical operations, regulatory affairs, and data management, to ensure timely and successful completion of clinical trials

Education

• Enugu State University of Science and Technology

  Bachelor's degree