Found Description
Join Prevail as a Clinical Research Associate specializing in oncology for high-impact Breast Cancer studies. This contract role offers both remote and on-site monitoring responsibilities across Canada.
As a seasoned Clinical Research Associate, you will oversee the management of clinical projects from initiation through close-out. Your expertise will guide site qualification and ensure adherence to protocols and regulatory standards. This role is ideal for diligent professionals who can assess site performance and maintain patient confidentiality through rigorous oversight.
Key Responsibilities:
• Perform monitoring, site management, and audits as required
• Ensure compliance with ICH-GCP and SOPs during studies
• Document essential activities and follow up on compliance
• Maintain ISF and TMF accuracy throughout the project lifecycle
• Collaborate with local staff and Sponsor affiliates
Requirements:
• Comprehensive understanding of ICH and GCP guidelines
As a seasoned Clinical Research Associate, you will oversee the management of clinical projects from initiation through close-out. Your expertise will guide site qualification and ensure adherence to protocols and regulatory standards. This role is ideal for diligent professionals who can assess site performance and maintain patient confidentiality through rigorous oversight.
Key Responsibilities:
• Perform monitoring, site management, and audits as required
• Ensure compliance with ICH-GCP and SOPs during studies
• Document essential activities and follow up on compliance
• Maintain ISF and TMF accuracy throughout the project lifecycle
• Collaborate with local staff and Sponsor affiliates
Requirements:
• Comprehensive understanding of ICH and GCP guidelines
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