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 Positive Pharmacoepidemiology Practice (GPP) and protocol com...