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Clinical Research Associate

Piper Companies

Montreal

Remote

CAD 90,000 - 120,000

Full time

2 days ago
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Job summary

Piper Companies is looking for a Clinical Research Associate (CRA) to ensure compliance and monitor clinical trials across Canada. The role requires at least 2 years of oncology monitoring experience and a bachelor's degree in a life sciences field. You will manage site communication, support recruitment efforts, and maintain documentation. The position offers a competitive salary and the opportunity to work with a global leader in clinical research.

Benefits

Comprehensive Benefits: Medical, Dental, Vision
401K
Sick leave if required by law

Qualifications

  • At least 2 years of onsite oncology monitoring experience.
  • Experience in site management and clinical trial documentation.
  • Advanced degree preferred.

Responsibilities

  • Conduct site monitoring visits to ensure compliance.
  • Support subject recruitment and manage communication with study sites.
  • Track study progress and maintain accurate site documentation.

Skills

Oncology monitoring experience
Knowledge of GCP and ICH guidelines
CTMS proficiency
Strong patient recruitment skills

Education

Bachelor's degree in life sciences, nursing, or a related field

Tools

Microsoft Office Suite

Job description

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Piper Companies is seeking a Clinical Research Associate (CRA) to join a global leader in clinical research and healthcare analysis for a remote position. The Clinical Research Associate (CRA) will monitor and participate in clinical trials across the country 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:

  • 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: $90,000-$120,000
  • 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 2/28. Applications for this job will be accepted for at least 30 days from the posting date.

Seniority level
  • Seniority level
    Entry level
Employment type
  • Employment type
    Full-time
Job function
  • Job function
    Research, Analyst, and Information Technology
  • Industries
    Business Consulting and Services

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