Senior Clinical Research Associate
$108,576–$135,720 year
On-site · Vancouver, British Columbia, Canada
Job Summary
Lead on-site monitoring visits across Oncology, Hematology, Prostate Cancer and Lung Cancer programs, ensuring ICH-GCP compliance and site readiness; maintain and reconcile CTMS/eTMF documents; support site staff training and compliance; monitor patient safety with AE/SAE/PQC reporting; manage drug accountability and storage/destruction; assist with site budgets and payments; collaborate with cross-functional teams (CTAs, LTMs, CTMs); travel about 50% to conduct monitoring visits and support recruitment and data quality across multiple therapeutic areas.
Required Qualifications
- Bachelor’s degree in Life Sciences or equivalent, or qualified RN
- 3+ years of on-site monitoring experience in pharmaceutical or CRO industry
- Knowledge of Health Canada regulations and working with REBs
- Familiarity with ICH-GCP, local regulatory requirements, and clinical systems like CTMS and eTMF
- Ability to travel approximately 50% for on-site monitoring visits
- Based in Vancouver, BC or eligible to work in Canada
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