Responsibilities will include identification and screening of eligible study subjects, assisting in the Informed Consent process, assisting Investigators in the assessment and monitoring of study subjects, maintaining essential study documents and collection/submission of the data required by each study protocol.
Candidates should possess a health sciences degree (BSc, MSc or PhD). Related experience in clinical trials and an understanding of good clinical practice (GCP) regulations is an asset. Excellent interpersonal, communication and organizational skills are mandatory.