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 queriesRequirements:
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 practicesLeverage your skills in ensuring successful Oncology trials at PXL FSP.#J-18808-Ljbffr

📌 Senior Clinical Research Associate Position Quebec City (Canada)
🏢 Parexel
📍 Canada