Top Tech Jobs & Startup Jobs in Montreal

Home-based CRA II responsible for monitoring Phase I-IV oncology trials. Conduct site selection, initiation, monitoring and close-out visits; train site staff on protocols and EDC; ensure data integrity, regulatory document collection, IP accountability, and prepare monitoring reports. Travel 65-70%.

The Clinical Research Associate II monitors oncology clinical trials, conducts site visits, ensures compliance with regulations, and manages data integrity.

The Principal Biostatistician provides statistical support for clinical research, managing data collection, analysis and modeling, study protocol development, and compliance with regulatory standards.

Design and build modern web UIs with Vue 3 and Material Design, develop and deploy .NET Core APIs, ensure comprehensive unit test coverage, collaborate with product teams, and drive continuous improvement of development processes.

Ensure timely and accurate payroll processing, manage payroll taxes, prepare reports, and comply with regulations. Assist in audits and support policy changes.

As a Senior Network Engineer, you will implement and support complex hybrid networks, mentor Tier 2 engineers, and lead strategic network projects while ensuring alignment with security and performance standards.

The Clinical Research Associate will oversee clinical trials, ensure compliance with best practices, train staff, and manage site activities. Responsibilities include evaluating investigator capabilities, coordinating regulatory approvals, conducting monitoring visits, and maintaining data integrity throughout the study phases.

The Senior Clinical Research Associate coordinates clinical trials, monitors progress, ensures compliance with regulations, and trains site staff while collaborating with clinical teams to achieve study objectives.

Lead site monitoring and management for clinical trials, ensure GCP/ICH regulatory compliance, support recruitment and study progress, train and mentor site and clinical staff, manage documentation and site finances as required.

The Clinical Research Associate (CRA) prepares and manages clinical trials, oversees site progress, ensures compliance, and manages data integrity. Requires excellent communication and organizational skills, with a focus on clinical best practices.