Elevate your career with PXL FSP as a Senior Clinical Research Associate focused on Oncology in Montreal/Quebec. Ensure the highest standards of clinical trial execution and regulatory compliance.
This pivotal role encompasses investigator selection, site monitoring, and training initiatives. You will be responsible for managing essential documentation and ensuring readiness for inspections, all while fostering quality and efficiency in clinical trials. Your work will significantly impact patient outcomes and data integrity.
Key Responsibilities:
• Conduct selection and training of site staff
• Monitor clinical sites for compliance and data quality
• Finalize documentation for regulatory authorities and audits
• Drive site performance through regular evaluations
• Ensure timely resolution of study-related queries
Requirements:
• Bachelor’s degree in life sciences or equivalent
• Expert understanding of ICH-GCP and local laws
• Robust attention to detail and communication skills
• Willingness to travel for site visits
• Proven experience in clinical trial management practices
Leverage your skills in ensuring successful Oncology trials at PXL FSP.
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📌 Senior Clinical Research Associate Position (Quebec City)
🏢 Parexel
📍 Quebec City
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