This experienced cardiac technician and medical office & laboratory assistant has experience in Phase II, III, and IV clinical trials. She has been responsible for most aspects of clinical trials including patient recruitment, obtaining informed consents, data collection, CRFs and eCRFs as well as source documentation, obtaining pertinent blood samples as well as centrifuging and shipping of samples and specimens. She has excellent knowledge of ICH and GCP guidelines and has attended the Investigator Support Initiative Workshop re ICH/GCP. She has attended the McMaster University’s Clinical Research Co-ordinator’s course.
Sue is a certified cardiovascular and medical laboratory technician with diplomas in venipuncture as well. She has up to date certification for handling and shipping of diagnostic and infectious specimens. She has excellent knowledge of ICH and GCP guidelines.
Danny Xie is a clinical research coordinator with up to date certification for handling and shipping of diagnostic and infectious specimens. He has excellent knowledge of ICH and GCP guidelines as well as regulatory document management and eCRF completion. He has experience with venipuncture, IM and SC injections and performing ECGs.