Clinical Research Associate I: Site Monitoring & Trials

AbbVie Inc.

Edmonton

On-site

CAD 65,000 - 90,000

Full time

45 hours ago
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Benefits offered by this job

Professional development
Paid time off
Wellness spending account
Flexible health insurance
Bonus plan

Job summary

AbbVie Inc. in Edmonton is seeking an experienced Clinical Research Associate to advance our clinical research programs. You will partner with investigators and site staff to drive high-quality, compliant trials and ensure robust patient safety and data integrity.

This role focuses on site engagement, risk assessment, and adherence to ICH/GCP guidelines. You will collaborate across functions to optimize site performance, manage monitoring activities, and mentor junior CRAs as needed in a

Qualifications

  • Minimum 1 year of clinically related experience, with at least 6 months in clinical research monitoring.
  • Familiar with risk-based monitoring approaches and GCP/I CH guidelines.
  • Strong ability to collaborate across functions and manage site relationships.
  • Demonstrate ethical integrity and adherence to AbbVie standards.

Responsibilities

  • Serve as primary contact for investigative sites and provide protocol guidance.
  • Train and motivate site staff and investigators on trial goals and patient care principles.
  • Monitor site activities for protocol compliance, data integrity, and patient safety.

Skills

Clinical monitoring
Site engagement
Regulatory knowledge
Cross-functional collaboration
Risk assessment

Education

Bachelor’s degree in Life Sciences or health-related field

Tools

CRM software
CTMS / EDC systems

Job description

AbbVie Inc. in Edmonton is seeking an experienced Clinical Research Associate to advance our clinical research programs. You will partner with investigators and site staff to drive high-quality, compliant trials and ensure robust patient safety and data integrity.

This role focuses on site engagement, risk assessment, and adherence to ICH/GCP guidelines. You will collaborate across functions to optimize site performance, manage monitoring activities, and mentor junior CRAs as needed in a

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