Join our team as a Quality Control Associate dedicated to ensuring the integrity of clinical studies. You will focus on documentation review, quality assurance, and training initiatives to uphold research standards.
In this role, you will scrutinize study files and documentation post-completion, ensuring they meet all regulatory and protocol requirements. The Quality Control Associate collaborates with CRCs to ensure studies are executed with high quality and efficiency. Your oversight will support auditing processes and drive compliance across clinical trials.
Key Responsibilities:
• Assess study files for compliance with SOPs
• Facilitate the preparation of study documents
• Conduct regular observations of clinical practice
• Develop QC tools and checklists for reviews
• Address QC issues and support corrective actions
Requirements:
• Bachelor’s degree in a relevant field
• 1+ year of experience in clinical trials preferred
• Knowledge of health produ...