Become an integral part of ICON plc in Vancouver as a Senior Clinical Research Associate, focusing on Oncology and multiple therapeutic areas. Drive compliance and effective monitoring strategies to enhance patient safety in clinical trials.
As a Senior Clinical Research Associate, you will conduct comprehensive site visits and serve as the main communication link between investigation sites and the sponsor. A minimum of 3 years of experience in in office monitoring within the pharmaceutical or CRO industry is required. Your background in ICH-GCP and relevant systems will ensure superior site management and regulatory compliance.
Key Responsibilities:
• Lead site visits, ensuring compliance at each stage
• Document site activities and escalate any concerns




• Coordinate site staff training and maintain records
• Monitor patient safety and resolve data queries
• Oversee drug handling and patient recruitment efforts
Requirements:
• At least 3 years of monitoring experience
• Bachelor's degree in relevant field or RN qualification
• Knowledge of CTMS and eTMF systems
• Robust understanding of Health Canada regulations
• Willingness to travel for site monitoring visits
Utilize your research expertise with ICON plc to foster innovation in clinical development from Vancouver.
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📌 Vancouver Senior Clinical Research Associate Role
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📍 Vancouver