MR. FREDRICK OMITI OCHUODHO

About: Summary • Assertive and versatile professional with 7 years of experience in Clinical Research and Clinical Trials conduct and management and able to manage multiple projects, providing exceptional support to multilevel collaborators to drive teams to success and meet multiple goals and requirements. • Possesses working knowledge of ICH and GCP regulations and guidelines; IRB protocols Protocol translation , Standard Operating Procedure (SOP) writing and compliance, recruiting and screening of patients, completing Case Report Forms and Informed Consent Forms . • Recognized for integrity, being compassionate and excelling in diagnosis and possesses extensive experience in leadership and team player amongst staff. Highlights • Working knowledge of ICH and GCP regulations and guidelines; IRB protocols Protocol translation, Standard Operating Procedure (SOP) writing and compliance, recruiting and screening of patients, completing Case Report Forms and Informed Consent Forms. • Clinical Training: Site qualification, site initiation, source data verification (SDV), Adverse Event (AE) reporting, monitoring of sites, site budget management, coordination of subject participation, and communication with subjects. • Able to manage multiple projects, providing exceptional support to senior executives, project managers and multilevel collaborators to drive teams to success and meet multiple goals and requirements. • Excellent verbal and written communication skills and proven organizational and leadership skills. • Able to work in a fast-paced environment with tight timelines.