I am submitting my resume for consideration of the recent opening. I have a degree in science and got my CRA diploma (CRA Professional Development Program, Kriger Research Center, Inc.Clinical Trial Monitoring and Research Site Coordination, The International Conference on Harmonization (ICH), Good Clinical Practice (GCP) Guidelines).
I was working as a research associate at Jerry L Pettis Memorial Vet Hospital-Loma Linda (Musculoskeletal Disease Center) and University of California Davis. During my research program, I was involved in researches relating to inflammatory response, nutrition requirements related to innate and adaptive immune responses. Also, working volunteer with patients who suffer from cancer and neurodevelopmental disorder has made me passionate to contribute my knowledge to clinical research field.
Throughout my working as a part Member of clinical development team, managed assigned investigational study sites and performed quality reviews in order to compliance with protocol, SOPs, and data entry for human trial and pre-clinical trial management (Design, develop and execute in vitro and in vivo), protocol adjustment, bio molecular techniques, kit and supply management, data collecting and statistical analysis, responsible for releasing of new articles on new products (conduct researching on that new products and scientific sales representative in cooperate with commercializing team), I have acquired skills that make me perfect for taking part in clinical trial. I have learned how to not only conduct but to observe and being detail oriented! I look forward to hearing from you for an interview.
** I am a permanent resident (Green Card holder), bilingual and ready to learn fast and willing to accommodate frequent local, domestic or international business travel.