Clinical Operations

• Preparing and coordinating regulatory submissions to Health Canada, Research Ethics Boards (REBs), and Institutional Review Boards (IRBs).
• Completing and maintaining Clinical Trial Site Information (CTSI) documentation.
• Managing regulatory documents and study files to ensure compliance and inspection readiness.
• Supporting multiple clinical studies simultaneously (typically 15+ active protocols).
• Processing clinical trial invoices accurately and efficiently.
• Tracking study documentation, regulatory milestones, and operational deliverables.
• Working cross-functionally with clinical operations, regulatory, and study teams to ensure timely study execution.
• Maintaining accurate records within study systems and databases.
• Supporting study start-up, maintenance, and closeout activities while ensuring adherence to sponsor processes and regulatory requirements.

Clinical Operations Specialist – Bilingual English/French

• Manage day-to-day operations of an assigned team in Clinical Operations
• Oversee performance, coaching, and training of Clinical Research Associates and support personnel
• Ensure proper monitoring and compliance with SOPs, GCP, and regulatory requirements
• Drive resources allocation and monitor adherence to project timelines and quality metrics
• Identify quality issues and establish corrective action plans
• Support training development and conduct assessments of clinical operations personnel

Clinical Operations jobs in Canada

See all jobs on JobTailor

Clinical Operations Specialist – Bilingual English/French

Clinical Operations Manager