Enhance your clinical research career as a Senior Clinical Research Associate at IQVIA in Montreal. This bilingual role focuses on site management, monitoring, and protocol adherence. At IQVIA, you will perform essential site monitoring visits, manage project requirements, and ensure the integrity of research protocols.

The role demands at least three years of on-site monitoring experience and expertise in Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. You will collaborate with clinical staff, manage study progress, and mentor other team members to ensure successful project outcomes. Key Responsibilities:

- Conduct site monitoring visits and evaluations
- Manage subject recruitment plans in line with project needs




- Maintain communication with sites regarding project status
- Escalate quality issues and ensure regulatory compliance
- Create and manage documentation for site management Requirements:
- Bachelor’s degree in a scientific discipline or healthcare
- Minimum 3 years of site monitoring experience
- Knowledge of clinical research regulatory requirements
- Solid competency in Microsoft Office applications
- Bilingual in French and English Join IQVIA to make a significant impact in clinical research and patient outcomes.

📌 Clinical Trial Assistant (Clinical Trial Management) (Kirkland)
🏢 IQVIA
📍 Kirkland