OBJECTIVE STATEMENT: I am a motivated, resilient, and captivating persuasive individual, who loves nothing more than helping people resolve their problems or render assistance in every way possible. I am a service-oriented professional that is very confident when handling, enquiries, complaints and communications. I am a team player, who can work to timely demands and effectively manage multiple workloads. I want to work in Clinical Research because I believe it is the heartbeat of medicine and I want to be part of the life changing innovation that brings hope and give them second chance on a new lease on life.
Reading, Writing, Music and Movies.
Clinical Research Training Comprehensive 80hour Training that covers core competences including but not limited to: FDA regulations including 21CFR Parts 11, 50, 54, 56 and the Common Rule ICH GCP E6 R(2) Informed Consent Process GDP following ALCOA-C principles Identification and reporting of AEs and SAEs Clinical Trial Operations from feasibility through close-out. Data Management Comprehension and Execution of Clinical Trial Protocols Quality Assurance, Monitoring and Query Resolution Maintaining regulatory binder, housing essential documents including but not limited to 1572, DOA, Source documents, and other Investigator Site File (ISF) documents