Clinical Research Associate II

3 days ago

Montreal, Quebec, Canada Piper Companies Full time

Piper Companies
is seeking a
Clinical Research Associate
(CRA) to join a global leader in clinical research and healthcare analysis for a
hybrid permanent position
located in
Montreal, Quebec
. The
Clinical Research Associate
(CRA) will monitor and participate in clinical trials across the region for a leading Clinical Research Organization.

Responsibilities of the Clinical Research Associate include:

  • Conduct site monitoring visits to ensure compliance with GCP, ICH, and regulatory guidelines.
  • Support subject recruitment and adapt recruitment plans as needed.
  • Provide protocol training and manage communication with study sites.
  • Assess site adherence to protocol and regulatory requirements, reporting quality issues.
  • Track study progress, including regulatory approvals, enrollment, data collection, and query resolution.
  • Maintain accurate site documentation, including visit reports and regulatory files.

Qualifications for the Clinical Research Associate include:

  • Must be bilingual (French & English)
  • At least 2 years of onsite oncology monitoring experience
  • Proficiency in CTMS, EDC, and Microsoft Office Suite.
  • Strong knowledge of GCP, ICH guidelines, and regulatory requirements.
  • Experience in site management, patient recruitment, and clinical trial documentation.
  • Strong therapeutic and protocol knowledge in Phase 1 oncology trials.
  • Bachelor's degree in life sciences, nursing, or a related field (advanced degree preferred).

Compensation for the Clinical Research Associate:

  • Salary Range: $100,000-$120,000/year (CAD)
  • Comprehensive Benefits: Medical (Cigna), Dental (Guardian), Vision (VSP), sick leave if required by law, and 401K (Voya through ADP)

This job opens for applications on 10/19/25. Applications for this job will be accepted for at least 30 days from the posting date.
Keywords: clinical research, clinical trials, GCP, regulatory compliance, clinical monitoring, data collection, site management, protocol adherence, patient recruitment, adverse event reporting, clinical study, documentation, IRB submissions, clinical trial management, data analysis, quality assurance, clinical operations, SOP, FDA regulations, ICH guidelines, electronic data capture, clinical trial design, oncology

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