Clinical Research Coordinator at The IMA Group (IMA Clinical Research) with expertise in patient recruitment, adverse event reporting and maintaining subject records. Proven track record in enhancing patient safety and ensuring compliance with ICH/GCP and FDA regulations. Strong organizational skills and adept in electronic data capture, contributing to the timely completion of clinical trials.
GCP (Good Clinical Practice)
IATA shipping of category A, Infectious substance affecting humans.
IATA shipping of category B, Biological Substance
Ethics and Human Subject Protection