Clinical Research Associate I - Remote

Overview

As a Clinical Research Associate I at AbbVie, you will be part of a dedicated team focused on conducting clinical trials that adhere to regulatory standards and ensure the safety of study participants.

In Short

• Support the organization and execution of clinical trials.
• Manage activities across multiple investigative sites.
• Ensure compliance with federal regulations and Good Clinical Practices.
• Participate in site qualification and training.
• Facilitate quality assurance audits and inspections.
• Assist with clinical trial applications and budget preparation.
• Communicate effectively with study site personnel.
• Maintain accurate reporting of study progress.
• Work collaboratively within a dynamic environment.
• Fluency in French and English is required.

Requirements

• Life-science or healthcare-related qualification or equivalent experience.
• Preferred one year of clinically-related experience.
• Knowledge of ICH/GCP guidelines and clinical research.
• Strong organizational and planning skills.
• Ability to communicate clearly and address issues effectively.
• Demonstrated business ethics and integrity.
• Occasional availability for training at the head office in St-Laurent, QC.
• Fluency in French and English.

Benefits

• Opportunity to work with a leading pharmaceutical company.
• Engagement in innovative clinical research.
• Collaborative and inclusive work environment.
• Professional development opportunities.
• Commitment to diversity and equal opportunity.