Chukwudi Opara

About Chukwudi Opara

I am a Clinical Research Associate with 4 years experience in the Clinical research industry. As a Clinical Research Associate, I perform and coordinates assigned aspects of clinical monitoring process in accordance with GCP. I have experience as a Assistant Clinical Research Associate/ Remote Site Monitor in a Phase Ia/Ib Hematology/Oncology study, were I performed remote site management and monitoring activities on assigned projects per company policy for reviewing study data, FDA guidelines, and ICH GCPsAlso, I worked as a Clinical Research Assistant in a Endocrinology/ metabolic Diseases, Cardiology/ Vascular Diseases, and Vaccine studies. I am Skilled in Analytical Skills, Microsoft Word, Databases, Commercial Banking, and Microsoft Access. Strong research professional with a Bachelor of Science - BS focused in Biomedical Sciences, General from Florida State College-Jacksonville.

Experience

1. Clinical Research Associate Ii

   Ppd

   Apr 2024 — Present

   Perform and coordinate all aspects of the clinical monitoring and site management process. Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation. Acts as a site processes specialist, ensuring that the trial is conducted by the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects\' rights, well-being, and data reliability. Perform and coordinate all aspects of the clinical monitoring and site management process. Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation. Acts as a site processes specialist, ensuring that the trial is conducted by the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects\' rights, well-being, and data reliability.

Education

• Florida State College at Jacksonville

  Bachelor of Science - BS, Biomedical Sciences, General

  2013 — 2018