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Benefits offered by this job
Health insurance
Retirement planning
Employee Assistance Programme
Annual leave entitlements
Job summary
A leading clinical research organization in Toronto seeks an experienced Clinical Research Associate to serve as the primary contact for investigational sites. The ideal candidate will ensure compliance, conduct monitoring visits, and support subject recruitment. A Bachelor’s in Life Sciences and 2+ years of relevant experience are required. Excellent benefits and a collaborative environment await you.
Qualifications
2+ years of on-site monitoring experience in the pharmaceutical or CRO industry.
Knowledgeable in Health Canada regulations and working with Research Ethics Boards (REBs).
Experience across multiple therapeutic areas, ideally including Oncology and Hematology.
Responsibilities
Serve as the primary point of contact between investigational sites and the sponsor.
Conduct site visits including selection, initiation, and monitoring.
Ensure site compliance with ICH-GCP and other regulations.
Skills
On-site monitoring
Knowledge of ICH-GCP
Problem-solving skills
Clear communication
Education
Bachelor’s degree in Life Sciences
Tools
CTMS
eTMF
Job description
A leading clinical research organization in Toronto seeks an experienced Clinical Research Associate to serve as the primary contact for investigational sites. The ideal candidate will ensure compliance, conduct monitoring visits, and support subject recruitment. A Bachelor’s in Life Sciences and 2+ years of relevant experience are required. Excellent benefits and a collaborative environment await you.