Senior Project Manager - Cardiometabolic

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Senior Project Manager - Cardiometabolic based in Canada.

This role sits within global clinical research project management, focusing on the end-to-end delivery of complex clinical trials in the cardiometabolic therapeutic area. The position plays a key role in ensuring studies are executed with rigor, compliance, and operational excellence from start-up through closeout. You will lead cross-functional study teams, coordinating scientific, operational, and financial activities to meet strict timelines and quality standards. The environment is fast-paced and highly collaborative, bringing together clinical experts, sponsors, and functional leaders across regions. This is a highly visible role where strong leadership directly impacts study outcomes and patient-facing innovation. It offers the opportunity to work in a mission-driven setting focused on advancing treatments in Cardiometabolic disease. The role is best suited for a proactive project leader who thrives in complex, global clinical environments.

• Lead full lifecycle management of global clinical trials within the cardiometabolic area, ensuring delivery from study start-up through closeout while meeting scope, timeline, budget, and quality expectations
• Coordinate cross-functional teams including clinical operations, data management, biostatistics, regulatory, and vendor partners to ensure aligned execution of study plans
• Oversee project financials, including budgeting, forecasting, and cost control activities, ensuring financial health across assigned studies
• Manage risk identification, mitigation planning, and issue resolution to maintain study continuity and regulatory compliance
• Serve as the primary point of contact for stakeholders and sponsors, providing clear communication on project status, milestones, and performance metrics
• Drive operational excellence by implementing best practices, optimizing workflows, and ensuring adherence to global clinical trial standards

Requirements

• Bachelor’s degree in Life Sciences or related field; advanced degree preferred
• 6–7+ years of industry experience with at least 5 years in clinical project management within a CRO or pharmaceutical environment
• Strong expertise in managing global clinical trials, ideally within cardiometabolic, cardiovascular, metabolic, or related therapeutic areas
• Solid understanding of clinical trial processes, regulatory requirements, and GCP standards
• Demonstrated ability to manage budgets, timelines, and multi-disciplinary teams in a matrix environment
• Excellent communication, leadership, and stakeholder management skills, with the ability to influence across global teams
• Strong problem-solving mindset with the ability to perform effectively in high-pressure, deadline-driven environments

Benefits

• Competitive base salary aligned with experience and market benchmarks
• Comprehensive medical, dental, and vision insurance coverage
• Retirement savings plans with company contributions (where applicable)
• Generous paid time off and holiday programs
• Flexible remote work arrangements within the United States
• Opportunities for career progression in a global clinical research environment
• Exposure to cutting-edge clinical studies across major therapeutic areas