Senior Clinical Research Associate - Oncology - Canada - FSP
Remote · Ontario, Canada or Quebec, Canada
Job Summary
Senior Clinical Research Associate responsible for the delivery of studies at allocated sites in Canada (Ontario/Quebec) with monitoring visits, site qualification, regulatory submissions, training investigators, ensuring ICH-GCP compliance, CTMS data updates, risk-based monitoring, and collaboration with Local Study Team and LSAD. Requires 5+ years of CRA experience in CRO/Pharma, oncology monitoring experience, Bachelor’s degree, ability to travel, and English plus local language proficiency.
Required Qualifications
- Bachelor’s degree (life sciences or related field)
- 5+ years of direct Monitoring / CRA experience in a CRO or Pharma organization
- 2+ years direct Oncology Monitoring / CRA experience in a CRO or Pharma organization
- Familiar with risk-based monitoring including remote monitoring
- Excellent knowledge of ICH-GCP; basic knowledge of GMP/GDP
- Good regulatory knowledge and ability to interact with site staff and regulators
- Ability to travel; valid driving license per country requirements
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