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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.
Accountabilities
- 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
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