• Performed patient Assessments, Collected and analyzed data, and prepared reports. • Maintained up-to-date tracking logs for all aspects of clinical research activities.• Gathered and reviewed Study data. • Reviewed CRFs for completeness and accuracy before database entry.• Facilitated Resolutions of the protocol of deviation or violations reported by sites or defects through monitoring activities. • Involved in the informed consent process during the subject involved in the study.• Data entry in the Specified software. Knowledge about GCP guidelines. • Assisted in preparing periodic reports summarizing the progress of clinical studies. • Developed and maintained accurate and timely study databases. • Monitored patient's safety during clinical trials according to established guidelines.