Location
vancouver, metro vancouver regional district, Canada
Posted
July 17, 2026
Job Description
Elevate your impact as an Oncology Clinical Research Associate at ICON plc in Vancouver. Apply your extensive monitoring experience in a pivotal role supporting clinical trials and patient safety.
As a Senior Clinical Research Associate, you will be responsible for maintaining compliance with Health Canada regulations while managing site interactions. This position requires a strong background in clinical research, particularly in oncology, and at least three years of relevant experience in a CRO or pharmaceutical setting.
Key Responsibilities:
ā¢ Act as the key liaison between sites and sponsors
ā¢ Conduct comprehensive site visits including initiation and routine checks
ā¢ Ensure compliance with ICH-GCP and local regulations
ā¢ Document progress and monitor safety reporting
ā¢ Track budgets and assist with site payment processes
Requirements:
ā¢ Over 3 years of clinical research experience
ā¢ Bachelorās degree in Life Sciences or equivalent
ā¢ Knowledge of CT...
As a Senior Clinical Research Associate, you will be responsible for maintaining compliance with Health Canada regulations while managing site interactions. This position requires a strong background in clinical research, particularly in oncology, and at least three years of relevant experience in a CRO or pharmaceutical setting.
Key Responsibilities:
ā¢ Act as the key liaison between sites and sponsors
ā¢ Conduct comprehensive site visits including initiation and routine checks
ā¢ Ensure compliance with ICH-GCP and local regulations
ā¢ Document progress and monitor safety reporting
ā¢ Track budgets and assist with site payment processes
Requirements:
ā¢ Over 3 years of clinical research experience
ā¢ Bachelorās degree in Life Sciences or equivalent
ā¢ Knowledge of CT...