Senior Clinical Project Manager

CanadaFull-timeCA$125k–CA$175kPosted Jul 13, 2026
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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 Clinical Project Manager based in Canada.

This role offers the opportunity to lead complex clinical research initiatives within a fast-growing and collaborative environment.
You will oversee global and regional clinical projects, ensuring successful delivery from planning through completion.
The position combines strategic project leadership, cross-functional coordination, and client partnership.
You will work closely with clinical, regulatory, data, and operational teams to drive high-quality outcomes.
Your expertise will directly contribute to advancing innovative therapies and medical solutions.
This is an impactful opportunity for an experienced clinical research professional who thrives in a dynamic setting and enjoys solving complex challenges.

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

This role offers the opportunity to lead complex clinical research initiatives within a fast-growing and collaborative environment.
You will oversee global and regional clinical projects, ensuring successful delivery from planning through completion.
The position combines strategic project leadership, cross-functional coordination, and client partnership.
You will work closely with clinical, regulatory, data, and operational teams to drive high-quality outcomes.
Your expertise will directly contribute to advancing innovative therapies and medical solutions.
This is an impactful opportunity for an experienced clinical research professional who thrives in a dynamic setting and enjoys solving complex challenges.

Accountabilities:

    The Senior Clinical Project Manager will take ownership of end-to-end project delivery, ensuring clinical research programs are executed on time, within budget, and according to quality standards. The role requires strong leadership, stakeholder management, and the ability to coordinate multidisciplinary teams across clinical development activities.

    • Lead the planning, execution, monitoring, and closure of Phase I–IV clinical trials while ensuring compliance with applicable regulations, guidelines, and quality standards.
    • Manage cross-functional project teams across clinical operations, statistics, data management, regulatory submissions, medical writing, vendor management, and other supporting functions.
    • Develop and maintain detailed project plans, timelines, budgets, resource forecasts, and risk mitigation strategies.
    • Track project progress, identify issues or deviations, and implement corrective actions to ensure successful delivery.
    • Prepare and present project status reports, including milestones, risks, financial performance, and operational updates, to internal and external stakeholders.
    • Act as the primary project management contact for clients, supporting communication, decision-making, scope alignment, and issue resolution.
    • Manage project budgets, resource allocation, and financial reconciliation while identifying opportunities for process improvement and operational efficiency.
    • Facilitate project meetings, document key decisions, and ensure effective follow-up on action items.
    • Support proposal development, scope definition, budgeting activities, and contract administration when required.
    • Build strong client relationships and identify opportunities to support future business growth.
    • Contribute to continuous improvement initiatives, including the development of project management processes, procedures, and quality standards.
    • Travel occasionally, including potential international travel, as required for project activities.
    • Requirements:

      The ideal candidate is an experienced clinical research leader with a strong background in managing complex pharmaceutical, biotechnology, or CRO projects. You should combine scientific knowledge, project management expertise, and excellent communication skills to successfully collaborate with diverse teams and stakeholders.

      • Bachelor’s or Master’s degree in life sciences, health sciences, or a related field.
      • More than 10 years of experience in clinical research and development within a pharmaceutical, biotechnology, healthcare, or CRO environment.
      • Minimum of 7 years of clinical project management experience with demonstrated expertise in managing clinical trial activities.
      • Experience overseeing Phase I–IV clinical studies from initiation through regulatory submission and completion.
      • Strong knowledge of ICH guidelines and regulatory requirements, including FDA, Health Canada, EMA, and other applicable standards.
      • Experience managing cross-functional clinical activities, including site selection, study start-up, clinical operations, data management, statistical programming, IWRS, regulatory submissions, and vendor oversight.
      • Oncology clinical research experience is highly preferred.
      • Previous clinical trial monitoring experience, including study initiation, monitoring, and close-out activities, is an asset.
      • Demonstrated ability to lead teams, manage resources, and deliver projects within defined timelines and budgets.
      • Strong financial management skills, including budget planning, forecasting, cost tracking, and change order management.
      • Excellent written and verbal communication, negotiation, and presentation skills.
      • Strong problem-solving abilities with experience managing risks, conflicts, and complex stakeholder environments.
      • Ability to build trusted relationships with clients and internal teams.
      • Benefits:

        • Competitive estimated salary range of $125,000 – $175,000.
        • Comprehensive benefits package including medical, dental, and vision coverage.
        • Life and accidental death & dismemberment insurance.
        • Short-term and long-term disability coverage.
        • Tuition reimbursement and professional development support.
        • Fitness reimbursement and employee assistance program (EAP).
        • Retirement savings program with employer-supported benefits.
        • Generous paid time off and sick leave.
        • Performance-based bonus opportunities.
        • Flexible work options, including remote work from anywhere in Canada.
How Jobgether works: We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team. We appreciate your interest and wish you the best!  Why Apply Through Jobgether?    Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time.     #LI-CL1

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