A leading clinical research network is hiring a Regulatory Specialist in Toronto, Ontario. This full-time role involves preparing and submitting regulatory documents essential for clinical trials, ensuring compliance with regulations. Candidates should have 1-3 years of clinical research experience, strong organizational skills, and familiarity with ICH/GCP and FDA requirements. The role offers an opportunity to contribute to efficient trial processes and facilitate collaboration among various stakeholders. Join a mission-driven team dedicated to advancing scientific research while maintaining a focus on quality and care.
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