Responsibilities
Conduct quality control reviews of clinical trial documentation for accuracy, consistency, and completeness, following study-specific plans, company procedures, and applicable regulations. Document and communicate findings, follow up on issues through resolution, maintain training records, and support staff training as appropriate.
Requirements
The posting does not specify formal education or years of experience; it describes an entry-level role performed under direction and guidance. The role requires maintaining knowledge of relevant US, Canadian, and European GxP and ICH regulations and following company SOPs and Good Clinical Practice guidelines.
