Manager, Monitoring & Site Management (Canada)

Alimentiv is a global CRO with a singular focus: advancing therapies for patients with gastrointestinal diseases. GI is our WHY and for more than 30 years that purpose has driven our scientific rigour, operational excellence, and deep therapeutic expertise, including supporting more than 70% of IBD compounds in development. We operate as a private, profit-with-purpose company, channeling our commercial success back into scientific research, technology, and our people. With approximately 700 people across multiple countries and three service lines, we are growing deliberately, and the capability of our leaders and our organization is central to how we get there. If you want to do meaningful work, build something real, and invest back in research that changes lives — we want to meet you! Job Overview The Manager, Monitoring & Site Management is responsible for the day-to-day leadership and delivery of the Clinical Monitoring function, with responsibility for Clinical Operations Leads and associated contractor resources. This role oversees resource planning, staff development and performance, clinical monitoring quality, regulatory compliance, process improvement and operational delivery. Working closely with project teams, sponsors and internal stakeholders, the Manager provides clinical monitoring expertise throughout the project lifecycle and ensures services are delivered to a high standard, on time and in accordance with regulatory requirements, industry best practices and organizational objectives. Key Responsibilities • Lead the day-to-day delivery of the Clinical Monitoring function, ensuring high-quality, timely and compliant services across assigned projects. • Manage and develop Clinical Operations Leads, including resource planning, work allocation, training and development, employee engagement and performance management. • Ensure appropriate staffing levels across projects, balancing operational requirements, team capacity and project priorities. • Partner with clinical monitoring and project leadership to develop and oversee project-specific strategies and processes relating to site selection, monitoring, ICH-GCP compliance and global project delivery. • Provide oversight and support for the identification, escalation and resolution of site, sponsor and clinical monitoring issues. • Drive the development and continuous improvement of policies, procedures, tools and processes supporting Clinical Monitoring activities. • Partner with internal stakeholders, sponsors and research sites to identify opportunities for improvement and support the implementation of new technologies and processes. • Identify, engage and manage independent contractor resources, including recruitment, contract support, training, cost monitoring, compliance and performance management. • Ensure Clinical Monitoring activities comply with applicable regulations, ICH-GCP, organizational procedures and industry best practices. • Provide Clinical Monitoring expertise to project teams and Business Development throughout the project lifecycle, from the bidding process through project delivery and reporting to sponsors. Skills & Qualifications • College diploma or university degree in a relevant field, preferably Health Sciences or Life Sciences; SoCRA and/or ACRP certification/designation is considered an asset. • Minimum 4–6 years of relevant clinical research/clinical monitoring experience with substantial ongoing training. • Demonstrated experience managing CRA or Clinical Monitoring staff, including performance management, resource planning and staff development. • Proven ability to train, mentor and support colleagues in both one-to-one and team settings. • Strong knowledge of ICH-GCP, applicable clinical research regulations and g