Overview
Clinical Trials Site Activation Specialist Jobs in Quebec, Canada at Pfizer, S.A. de C.V
Location: Quebec
Join Pfizer in Canada as a Clinical Trials Site Activation Specialist. Lead the start-to-finish operational activities essential for successful clinical research.
In your role as a Site Activation Partner I, you will oversee the regulatory, ethical, and essential documentation needed for clinical trials. This position calls for strong organizational skills and the ability to communicate effectively with diverse stakeholders throughout the study lifecycle. You will be instrumental in ensuring compliance with regulatory standards and supporting site activation efforts.
Key Responsibilities:
• Coordinate Investigator Initiation Packages for trials
• Manage updates and approvals for trial documents
• Facilitate communication with study teams and investigator sites
• Mentor new staff and represent the role in initiatives
• Ensure compliance across multi-country studies
Requirements:
• Diploma with relevant combination of education and experience
• Minimum 4 years in clinical trial environments
• Knowledge of clinical methodology and regulations
• Bilingual in English and French preferred
• Ability to learn and use various systems
Utilize your expertise in clinical trials to support innovative breakthroughs at Pfizer.
#J-18808-Ljbffr
Title: Clinical Trials Site Activation Specialist
Company: Pfizer, S.A. de C.V
Location: Quebec, Canada
Category: