Project Manager I, RWE

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

This role focuses on the coordination and delivery of real-world evidence (RWE) study operations within a clinical research environment, supporting the successful execution of observational and post-market research projects. You will manage study activities across multiple internal teams and external vendors, ensuring timelines, quality standards, and regulatory compliance are consistently met. The position plays a key role in maintaining trial master file (TMF) readiness, supporting financial tracking, and contributing to study reporting and milestone delivery. You will also collaborate with stakeholders to ensure smooth study execution, risk mitigation, and operational efficiency. In addition to project oversight, you will contribute to vendor management, resource coordination, and process improvements across studies. This is a highly collaborative, detail-oriented role ideal for professionals who thrive in structured, data-driven clinical environments.

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

This role focuses on the coordination and delivery of real-world evidence (RWE) study operations within a clinical research environment, supporting the successful execution of observational and post-market research projects. You will manage study activities across multiple internal teams and external vendors, ensuring timelines, quality standards, and regulatory compliance are consistently met. The position plays a key role in maintaining trial master file (TMF) readiness, supporting financial tracking, and contributing to study reporting and milestone delivery. You will also collaborate with stakeholders to ensure smooth study execution, risk mitigation, and operational efficiency. In addition to project oversight, you will contribute to vendor management, resource coordination, and process improvements across studies. This is a highly collaborative, detail-oriented role ideal for professionals who thrive in structured, data-driven clinical environments.

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!

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