Description
AbCellera is hiring a Senior Clinical Research Associate to serve as the primary liaison between the sponsor and investigative sites, overseeing complex clinical trials from site selection through close-out. The role owns monitoring activities, source data verification, investigational product accountability, protocol deviations, risk-based monitoring, audit readiness, and site performance, while mentoring junior CRAs and collaborating with data, project management, and medical teams. Candidates need a life sciences, nursing, pharmacy, or related degree, at least 10 years of CRA monitoring experience, extensive site-selection and initiation experience, advanced ICH-GCP and regulatory knowledge, strong judgment and stakeholder-management skills, and willingness to travel to clinical sites in Canada and the United States 60–70% of the time; bilingual French/English ability is required for Quebec sites. The position offers base salary, equity, an annual bonus, a CAD 1,500 annual Active Lifestyle Allowance, professional development, vacation, and comprehensive health benefits.
