Canada Clinical Research Associate — Oncology & Multi-TA Trials

ICON

Canada

On-site

CAD 80,000 - 110,000

Full time

14 days+

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Benefits offered by this job

Annual leave
Health insurance
Retirement planning
LifeWorks EAP
Life assurance
Childcare vouchers
Bike purchase
Gym membership discounts
Travel passes
Health assessments

Job summary

ICON plc is a world-leading healthcare intelligence and clinical research organization actively seeking a Clinical Research Associate to join our Canada team. The role involves monitoring trials, visiting sites, and collaborating with cross-functional teams to ensure data integrity and regulatory compliance throughout the study lifecycle.

The ideal candidate holds an advanced degree in life sciences, nursing, or medicine and has extensive CRA experience with strong organizational and

Qualifications

  • Advanced degree in life sciences, nursing, or medicine.
  • Extensive CRA experience with understanding of trial processes and regulatory requirements.
  • Proven ability to manage multiple sites and projects simultaneously.

Responsibilities

  • Monitor trial sites to ensure adherence to study protocols, regulatory requirements, and GCP standards.
  • Conduct site visits to assess site performance, resolve issues, and provide support for successful trial execution.
  • Collaborate with cross-functional teams to ensure timely and accurate data collection and reporting.
  • Provide training and guidance to site staff to maintain high standards of trial conduct.
  • Build and maintain effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Skills

Monitoring
Data integrity
Site management
Communication
GCP knowledge

Education

Advanced degree in life sciences or related field

Tools

Clinical trial software

Job description

ICON plc is a world-leading healthcare intelligence and clinical research organization actively seeking a Clinical Research Associate to join our Canada team. The role involves monitoring trials, visiting sites, and collaborating with cross-functional teams to ensure data integrity and regulatory compliance throughout the study lifecycle.

The ideal candidate holds an advanced degree in life sciences, nursing, or medicine and has extensive CRA experience with strong organizational and

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