|
|
|
|
She has excellent knowledge of ICH and GCP guidelines and has attended the Investigator Support Initiative Workshop re ICH/GCP. She is certified in the McMaster University’s Clinical Research Co-ordinator’s course.
She has been responsible for all 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.
|
|
THIS SITE IS INTENDED FOR CANADIAN USE ONLY AND NOT INTENDED FOR PATIENT RECRUITMENT. REQUESTS FOR INDIVIDUAL PATIENT CONSULTATIONS IS STRICTLY PROHIBITED AND REGRETFULLY CANNOT BE ANSWERED.
|