Clinical Research Associate

Piper Companies; Montreal; Remote; CAD 90,000 - 120,000; Full time

Job summary

A leading company in clinical research is looking for a Clinical Research Associate (CRA) for a remote position. This role involves monitoring clinical trials, ensuring compliance with regulations, and managing communication with study sites. Candidates should have oncology monitoring experience and a relevant degree. Competitive salary and comprehensive benefits are offered.

Benefits

Medical (Cigna)

Dental (Guardian)

Vision (VSP)

401K (Voya through ADP)

Qualifications

• At least 2 years of onsite oncology monitoring experience.
• Strong therapeutic and protocol knowledge in Phase 1 oncology trials.

Responsibilities

• Conduct site monitoring visits to ensure compliance with GCP, ICH, and regulatory guidelines.
• Track study progress, including regulatory approvals and data collection.

Skills

Oncology Monitoring

GCP

ICH Guidelines

Patient Recruitment

Education

Bachelor's degree in life sciences

Advanced degree preferred

Tools

CTMS

EDC

Microsoft Office Suite

Job description

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.