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The Principal Clinical System Designer leads all design responsibilities, supports library reuse, develops bid materials, trains junior staff, and collaborates on troubleshooting issues related to clinical trials.

The Feasibility Principal Analyst leads the feasibility strategy for clinical studies, analyzes data for insights, mentors junior team members, and collaborates cross-functionally to optimize trial execution.

The Global Study Manager oversees project management activities, leading teams to execute project plans, collaborating with stakeholders, and mentoring team members for successful project delivery.

As a Global Study Manager, you'll lead project execution, manage cross-functional teams, develop project plans, and mentor your team to ensure quality outcomes.

Oversee and monitor clinical trial sites to ensure GCP and protocol compliance, conduct site visits, resolve issues, ensure data integrity, train site staff and CRAs, collaborate with cross-functional teams, and maintain stakeholder relationships to support trial execution.

The manager will oversee operational planning, implement process improvements, manage KPIs, and coach team members to enhance efficiency.

As a Study Start Up Associate I, you will assist in preparing regulatory documents, coordinating approvals, maintaining records, supporting study teams, and participating in meetings related to clinical trials.

The Site Activation Partner facilitates clinical trial initiation, ensures regulatory compliance, and collaborates on developing necessary study documents.