CRA II - Eastern Canada (Onsite/Remote)

Premier Research; Quebec; Hybrid; CAD 70,000 - 90,000; Full time

Job summary

Premier Research is seeking a Clinical Research Associate II (Eastern Canada) to join our Clinical Monitoring, Site Management and SSU team. You will help biotech, medtech, and specialty pharma transform ideas into medicines and devices, with a focus on data integrity and patient safety.

Youll monitor sites across Eastern Canada (Ontario/Quebec), serving as the primary contact, coordinating TMF activities, and ensuring timelines and budgets. French fluency preferred; 70-85% travel expected.

Qualifications

• Undergraduate degree required or its international equivalent.
• Minimum of 2+ years of clinical research monitoring experience.
• Able to interact professionally with sites, clients, vendors and other teams.

Responsibilities

• Perform monitoring activities on site and remote for Phase I–IV trials and device trials.
• Ensure data validity, accuracy and safety per protocol and ICH-GCP/ISO 141155.
• Serve as primary contact for investigative sites; manage queries and TMF activities.
• Identify risks and retraining opportunities; plan day-to-day monitoring visits and reports.
• Travel 70–85% to sites, close to major airports, with 8 DOS per month target.

Skills

Data integrity

Site coordination

Communication

Travel readiness

French language

Education

Undergraduate degree

Job description

Premier Research is seeking a Clinical Research Associate II (Eastern Canada) to join our Clinical Monitoring, Site Management and SSU team. You will help biotech, medtech, and specialty pharma transform ideas into medicines and devices, with a focus on data integrity and patient safety.

Youll monitor sites across Eastern Canada (Ontario/Quebec), serving as the primary contact, coordinating TMF activities, and ensuring timelines and budgets. French fluency preferred; 70-85% travel expected.