Multicenter Clinical Trial Operations Lead

RI-MUHC | Research Institute of the MUHC | #rimuhc; Montreal; On-site; CAD 85,000 - 120,000; Full time

Job summary

RI-MUHC is seeking an experienced Clinical Trial Project Manager to oversee multicentre studies, including start-up, site management, regulatory compliance, and data coordination in Montreal. You will partner with sponsors, investigators, CRAs/Monitors, and labs to ensure timelines and quality.

You will lead onboarding, monitor recruitment, manage study logistics, and address operational risks in a fast-paced research environment dedicated to patient-centered medicine.

Qualifications

• Experience in multicentre clinical research start-up and site activation.
• Strong knowledge of regulatory requirements and submissions (REB/Nagano).
• Budget planning, revisions, and coordination with sponsors and sites.

Responsibilities

• Oversee study start-up, site activation, and regulatory documentation for multicentre studies.
• Coordinate preparation and follow-up of CTAs, Site Agreements, budgets, and revisions.
• Manage site regulatory submissions and follow-up queries and amendments.

Skills

Study Start-Up

Site Activation

Regulatory Submissions

Budget Management

Stakeholder Coordination

Clinical Monitoring

Data Management

Multicentre Trials

Job description

RI-MUHC is seeking an experienced Clinical Trial Project Manager to oversee multicentre studies, including start-up, site management, regulatory compliance, and data coordination in Montreal. You will partner with sponsors, investigators, CRAs/Monitors, and labs to ensure timelines and quality.

You will lead onboarding, monitor recruitment, manage study logistics, and address operational risks in a fast-paced research environment dedicated to patient-centered medicine.