Summary

The Clinical Research Associate will perform monitoring and site management activities for Phase I‑IV clinical research projects to assess the progress of clinical projects at assigned investigative/physician sites (either on site or remotely) and to ensure clinical projects are conducted, recorded, and reported in accordance with the protocol, Company and Sponsor standard operating procedures (SOPs), ICH‑GCP and/or all applicable local and federal regulatory requirements. We are looking for a seasoned CRA that has experience with Breast Cancer studies, lives in Canada (BC, Ontario, Quebec). Performs all tasks routinely and independently, seeking guidance as needed.

Essential Duties and Responsibilities

• Performs site qualification site initiation, interim monitoring, site management activities and close‑out visits (performed on‑site or remotely) ensuring regulatory, ICH‑GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol complian...