Oncology Senior Clinical Research Associate

Advance your career in clinical research as a Senior Clinical Research Associate specializing in Oncology at ICON plc in Vancouver. Engage with investigational sites, ensuring compliance and monitoring patient safety effectively.
In your role, you will be pivotal in liaising between investigational sites and the sponsor. Candidates must possess a Bachelor’s degree in Life Sciences or equivalent, along with over 3 years of on-site monitoring experience, preferably in Oncology or related therapeutic areas. Your expertise in ICH-GCP and regulations will guide compliance and documentation throughout the clinical trials.
Key Responsibilities:
• Conduct site visits including selection, initiation, and monitoring
• Ensure compliance with ICH-GCP and Health Canada regulations
• Monitor patient safety and handle AE/SAE reporting
• Document site progress and escalate issues
• Collaborate effectively with cross-functional teams
Requirements:
• 3+ years of on-site monito...