Top Tech Jobs & Startup Jobs in Montreal

The Senior Study Manager oversees clinical trial operations, managing teams, vendor interactions, budgets, timelines, and ensuring compliance and quality control throughout the study process.

The Senior Study Manager will oversee clinical trial activities, manage operational deliverables, vendor interactions, and ensure compliance with protocols and budgets while leading the Clinical Trial Team.

The Sr. Global Operations Quality Manager ensures compliance with quality standards in clinical trials, provides consultation, and supports inspection readiness activities while fostering collaboration between teams.

The Global Study Associate will support administrative functions for clinical studies, manage study documents, and ensure compliance while coordinating participant communications and meetings.

The Investigator Contracts Lead manages negotiation and maintenance of clinical trial agreements, ensuring compliance and timely execution while coordinating with internal and external stakeholders.

The Senior Clinical Research Associate will monitor clinical studies, ensuring compliance with protocols, regulations, and procedures, while also overseeing remote and on-site clinical trial progress.

As a Senior Statistical Programmer II, you will develop and validate statistical programs, collaborate with biostatisticians, and ensure compliance with regulatory standards.

The Clinical Trial Coordinator manages trial and site administration, document management, regulatory duties, budgeting, and meeting planning to support clinical research operations.

As a Senior Clinical Research Associate, you will monitor clinical studies, ensuring compliance with protocols and regulatory requirements. You will work both on-site at investigative sites and remotely, focusing on data integrity and patient safety.

Conduct site visits for clinical trials, oversee trial conduct, maintain relationships with site staff, and ensure compliance with regulations.