Clinical Research Associate II - Vancouver

As a CRA you will be joining the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence. What You’ll Be Doing: • 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 • Maintain up-to-date documentation in CTMS and eTMF systems • Support and track site staff training and maintain compliance records • Monitor patient safety, ensuring timely and accurate AE/SAE/PQC reporting • Support subject recruitment and retention efforts at the site level • Oversee drug accountability and ensure proper storage, return, or destruction • 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) • Collaborate with cross-functional partners including CTAs, LTMs, and CTMs You are: • Based in Vancouver, British Columbia • Eligible to work in Canada without visa sponsorship • 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 eTMF • A clear communicator, problem-solver, and collaborative team player • Willing and able to travel approximately 50% for on-site monitoring visits Apply tot his job