Senior Clinical Research Associate - Remote (Canada)

ICON San Antonio; Montreal; Remote; CAD 70,000 - 110,000; Full time

Job summary

ICON plc is seeking a Senior Clinical Research Associate (CRA) to monitor clinical studies from home across Canada. You will ensure trials are conducted, documented and reported in accordance with the protocol, SOPs, ICH-GCP and applicable regulations.

The role requires a Bachelor’s degree in a scientific/health field and 1+ years of monitoring experience; oncology monitoring is preferred. Expect travel up to 70% and collaboration with cross-functional teams to safeguard study quality and

Qualifications

• Bachelor’s degree in a scientific or health-related field or equivalent.
• 1+ years of clinical monitoring experience required for level 2; 3+ years for level 3.
• Oncology monitoring experience preferred.
• Ability to travel up to 70%.

Responsibilities

• Monitor progress of clinical studies at sites or remotely, ensuring trials are conducted, recorded, and reported per protocol and ICH-GCP.
• Ensure compliance with SOPs and regulatory requirements.
• Collaborate with study teams to ensure data quality and patient safety.

Skills

Clinical monitoring

ICH-GCP knowledge

Regulatory knowledge

Travel readiness

Education

Bachelor's degree in science/health

Job description

ICON plc is seeking a Senior Clinical Research Associate (CRA) to monitor clinical studies from home across Canada. You will ensure trials are conducted, documented and reported in accordance with the protocol, SOPs, ICH-GCP and applicable regulations.

The role requires a Bachelor’s degree in a scientific/health field and 1+ years of monitoring experience; oncology monitoring is preferred. Expect travel up to 70% and collaboration with cross-functional teams to safeguard study quality and