Join our FSP team as a Senior Clinical Research Associate with a focus on Oncology in Toronto, Canada. Leverage your monitoring expertise in a remote work environment to contribute to groundbreaking clinical trials.
With over four years of clinical monitoring experience, you will play a vital role in ensuring the highest standard of care for clinical trial participants. Your responsibilities will include site management, ensuring adherence to protocols, and supporting the integrity of study data. This role will see you engaging with both study staff and vendors, aligning everyone with project goals.
Key Responsibilities:
• Monitor clinical sites, ensuring all protocols are followed
• Maintain and manage study files and documentation
• Conduct monitoring visits, including pre-study assessments
• Verify compliance with informed consent and regulatory standards
• Report and manage Serious Adverse Events (SAEs) efficiently
Requirements:
• Degree or certification ...