As a CRA you will be joining the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence.
Serve as the primary point of contact between investigational sites and the sponsor
Conduct all types of site visits, including selection, initiation, routine monitoring, and close-out
Ensure site compliance with ICH-GCP, SOPs, and Health Canada regulations
Support and track site staff training and maintain compliance records
Support subject recruitment and retention efforts at the site level
Resolve data queries and drive timely, high-quality data entry
Document site progress and escalate risks or issues to the clinical team
Assist in tracking site budgets and ensuring timely site payments (as applicable)
A clinical research professional with 2+ years of on-site monitoring experience in the pharmaceutical or CRO industry
Experienced across multiple therapeutic areas, ideally including Oncology, Hematology, Prostate Cancer, Lung Cancer, and Early Phase/Phase 1
A graduate with a Bachelor’s degree in Life Sciences or equivalent, or a qualified RN
Knowledgeable in Health Canada regulations and working with Research Ethics Boards (REBs)
Proficient in ICH-GCP, local regulatory requirements, and clinical systems like CTMS and e TMF
