Clinical Research Associate Jobs in Quebec, Canada

The Clinical Research Associate II will oversee oncology clinical trials, ensuring sites follow protocols and regulations. Responsibilities include site visits, data monitoring, and regulatory compliance.

The Associate Clinical Project Management Director oversees clinical projects and research studies, ensuring compliance with global and local regulations. This role involves managing study execution from initiation to closure, coordinating cross-functional teams, and ensuring quality deliverables are met on time and within budget.

The Bilingual Patient Support Specialist provides clinical support and navigation assistance to patients, healthcare professionals, and pharmacists. This remote role involves handling inquiries, offering treatment guidance, and managing reimbursement processes.

Parexel’s Third Party Quality Lead (TPQL) drives quality risk management for clinical trial partners, ensuring GCP compliance and data integrity across global vendors and sites. The role leads quality discussions, audits, CAPA tracking, and continuous improvement initiatives, collaborating with vendor leads and oversight teams to uphold sponsor policies.

The Study Analyst will support real-world evidence studies for pharmaceutical clients, governments, and academic centers. Responsibilities include developing study documents, site selection, contract management, ethics committee liaison, site setup, data collection, and ensuring compliance with study protocols.