Clinical Trial Manager I

📋 Description

• Oversee clinical monitoring, site management, and central monitoring from activation through
• Ensure patient safety, protocol adherence, GCP/regulatory compliance, and data integrity.
• Monitor study progress, dashboards, and systems to identify risks impacting timelines, quality
• Lead risk mitigation activities and risk-based monitoring practices.
• Coordinate with multi-functional teams to ensure smooth handoffs and milestone achievement.

🎯 Requirements

• Bachelor’s degree, RN qualification, or equivalent experience in a related field.
• Experience in clinical trials and site management with oversight of teams and deliverables.
• Knowledge of GCP, ICH guidelines, and regulatory requirements.
• Ability to lead multidisciplinary teams toward milestones and operational objectives.
• Strong analytical, communication, and problem-solving skills; familiarity with trial systems and
• Willingness for moderate travel (~20%).

🎁 Benefits

• Fully remote position within Canada.
• Full-time employment.
• Opportunity to contribute to clinical research and development of therapies worldwide.
• Career development, supportive line management, and training opportunities.
• Exposure to international clinical programs and collaborative teams.