Join Sitero as a Senior Quality Assurance Associate with a hybrid work model in Mississauga. You’ll ensure compliance and quality in clinical studies while managing Trial Master Files and supporting teams.
Sitero is seeking a Senior Quality Assurance Associate to enhance its Clinical services and software solutions. This role focuses on quality checks, compliance oversight, and maintaining GCP standards in clinical trials. You will leverage your expertise in trial management and regulation adherence while collaborating with clinical operations teams.
Key Responsibilities:
• Perform quality checks on Trial Master File documents
• Review site-level essential documents and compliance
• Conduct routine internal quality reviews and audits
• Identify and log documentation errors or compliance gaps
• Assist with regulatory health authority inspections preparation
Requirements:
• Bachelor's degree in life sciences or related field
• 2-4 years experience in clinical research QA or TMF management
• Deep understanding of ICH-GCP guidelines
• Solid problem-solving and communication skills
• Ability to assess new regulations and standards impact
Enhance clinical trial quality by ensuring adherence to GCP with Sitero’s dedicated team.
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