Clinical Trial Assistant

We are seeking a Clinical trial Assistant for our client who is based in Laval, Quebec. In this role, you will assist the research team in planning, executing, and managing clinical studies, while maintaining the integrity, rigor, and compliance of study related activities. In addition, you will be responsible for contributing to the advancement of clinical research and the development of new therapies, with the goal of improving patients' quality of life. This is a permanent role on a hybrid work schedule (two days onsite) available immediately.

Responsibilities

• Regulatory compliance:
• Provide the necessary support for clinical trial management while complying with regulatory requirements, Good Clinical Practice (GCP), and International Conference on Harmonization (ICH) guidelines.
• Participate in the preparation and submission of trial documents to the Institutional Review Board (IRB).
• Colla...